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SNAR-B1 small NF90 (ILF3) associated RNA B1 [ Homo sapiens (human) ]

Gene ID: 100170224, updated on 13-May-2022

Summary

Official Symbol
SNAR-B1provided by HGNC
Official Full Name
small NF90 (ILF3) associated RNA B1provided by HGNC
Primary source
HGNC:HGNC:34317
See related
AllianceGenome:HGNC:34317
Gene type
snRNA
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See SNAR-B1 in Genome Data Viewer
Location:
19q13.33
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (50133745..50133864, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (53221168..53221287, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (50637002..50637121, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene small NF90 (ILF3) associated RNA A10 Neighboring gene small NF90 (ILF3) associated RNA A11 Neighboring gene uncharacterized LOC105372436 Neighboring gene small NF90 (ILF3) associated RNA B2 Neighboring gene small NF90 (ILF3) associated RNA D

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_024231.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC010624

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    50133745..50133864 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    53221168..53221287 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)