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SNORD56B small nucleolar RNA, C/D box 56B [ Homo sapiens (human) ]

Gene ID: 319139, updated on 12-Oct-2019

Summary

Official Symbol
SNORD56Bprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box 56Bprovided by HGNC
Primary source
HGNC:HGNC:19771
See related
Ensembl:ENSG00000207444
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
RNU56B

Genomic context

See SNORD56B in Genome Data Viewer
Location:
14q24.2
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (71398337..71398407)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (71865054..71865124)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984654 Neighboring gene uncharacterized LOC102724015 Neighboring gene PDZ domain containing 11 pseudogene Neighboring gene signal induced proliferation associated 1 like 1 Neighboring gene RNA, 7SL, cytoplasmic 683, pseudogene Neighboring gene uncharacterized LOC145474

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_001276.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC005994
    Related
    ENST00000384713.1

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_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    71398337..71398407
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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