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SNORA70B small nucleolar RNA, H/ACA box 70B [ Homo sapiens (human) ]

Gene ID: 100124537, updated on 12-Oct-2019

Summary

Official Symbol
SNORA70Bprovided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 70Bprovided by HGNC
Primary source
HGNC:HGNC:33618
See related
Ensembl:ENSG00000206937
Gene type
snoRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See SNORA70B in Genome Data Viewer
Location:
2p15
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (61417244..61417377, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (61644379..61644512, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374758 Neighboring gene chromosome 2 open reading frame 74 Neighboring gene activator of HSP90 ATPase homolog 2, pseudogene Neighboring gene ubiquitin specific peptidase 34 Neighboring gene uncharacterized LOC105377633 Neighboring gene exportin 1

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • SNORA70B snoRNA
  • small nucleolar RNA, H/ACA box 70B (retrotransposed)

NCBI Reference Sequences (RefSeq)

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_003707.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC016894
    Related
    ENST00000384210.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    61417244..61417377 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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