Canonical Allele Identifier: CA255622
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 10953
ClinVar RCV Id: RCV000011700
dbSNP Id: rs104894889
MyVariant Identifiers: chrX:g.30326777C>T (hg19) chrX:g.30308660C>T (hg38)
PubMed: PMID:7990958
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308660C>T , CM000685.2:g.30308660C>T GRCh38
NC_000023.10:g.30326777C>T , CM000685.1:g.30326777C>T GRCh37
NC_000023.9:g.30236698C>T NCBI36
NG_009814.1:g.5719G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.704G>A MANE Select ENSP00000368253.4:p.Trp235Ter
ENST00000378970.4:c.704G>A ENSP00000368253.4:p.Trp235Ter
NM_000475.4:c.704G>A NP_000466.2:p.Trp235Ter
NM_000475.5:c.704G>A MANE Select NP_000466.2:p.Trp235Ter
Search 100 bp 5'
Search 100 bp 3'