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SNORA36B small nucleolar RNA, H/ACA box 36B [ Homo sapiens (human) ]

Gene ID: 677818, updated on 21-Dec-2019

Summary

Official Symbol
SNORA36Bprovided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 36Bprovided by HGNC
Primary source
HGNC:HGNC:32629
See related
Ensembl:ENSG00000222370
Gene type
snoRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ACA36b

Genomic context

See SNORA36B in Genome Data Viewer
Location:
1q41
Exon count:
1
Annotation release Status Assembly Chr Location
109.20191205 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (220200546..220200676, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (220373888..220374018, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene isoleucyl-tRNA synthetase 2, mitochondrial Neighboring gene microRNA 194-1 Neighboring gene ribosomal protein S15a pseudogene 12 Neighboring gene RAB3 GTPase activating non-catalytic protein subunit 2 Neighboring gene microRNA 664a Neighboring gene sorting nexin 2 pseudogene 1 Neighboring gene mortality factor 4 like 1 pseudogene 1

Genomic regions, transcripts, and products

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_002994.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL445435
    Related
    ENST00000410438.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20191205

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    220200546..220200676 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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