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SNORD96B small nucleolar RNA, C/D box 96B [ Homo sapiens (human) ]

Gene ID: 692226, updated on 12-Oct-2019

Summary

Official Symbol
SNORD96Bprovided by HGNC
Official Full Name
small nucleolar RNA, C/D box 96Bprovided by HGNC
Primary source
HGNC:HGNC:32759
See related
Ensembl:ENSG00000208883
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
U96b

Genomic context

See SNORD96B in Genome Data Viewer
Location:
Xq23
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (110224989..110225060, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (109468217..109468288, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene transmembrane protein 164 Neighboring gene microRNA 3978 Neighboring gene uncharacterized LOC101928589 Neighboring gene AMMECR nuclear protein 1 Neighboring gene uncharacterized LOC105373312 Neighboring gene G protein subunit gamma 5 pseudogene 2

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_004379.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AY349596
    Related
    ENST00000386148.1

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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    110224989..110225060 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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