Canonical Allele Identifier: CA10376251
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs760506998
ExAC: X:30322677 T / G
gnomAD v2: X-30322677-T-G
gnomAD v4: X-30304560-T-G
MyVariant Identifiers: chrX:g.30322677T>G (hg19) chrX:g.30304560T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304560T>G , CM000685.2:g.30304560T>G GRCh38
NC_000023.10:g.30322677T>G , CM000685.1:g.30322677T>G GRCh37
NC_000023.9:g.30232598T>G NCBI36
NG_009814.1:g.9819A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*19A>C MANE Select ENSP00000368253.4:n.*19A>C
ENST00000378970.4:c.*19A>C ENSP00000368253.4:n.*19A>C
NM_000475.4:c.*19A>C NP_000466.2:n.*19A>C
NM_000475.5:c.*19A>C MANE Select NP_000466.2:n.*19A>C
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