Canonical Allele Identifier: CA10376314
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs747078429
ExAC: X:30326418 C / T
gnomAD v2: X-30326418-C-T
gnomAD v4: X-30308301-C-T
MyVariant Identifiers: chrX:g.30326418C>T (hg19) chrX:g.30308301C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308301C>T , CM000685.2:g.30308301C>T GRCh38
NC_000023.10:g.30326418C>T , CM000685.1:g.30326418C>T GRCh37
NC_000023.9:g.30236339C>T NCBI36
NG_009814.1:g.6078G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1063G>A MANE Select ENSP00000368253.4:p.Ala355Thr
ENST00000378963.1:c.178G>A ENSP00000368246.1:p.Ala60Thr
ENST00000378970.4:c.1063G>A ENSP00000368253.4:p.Ala355Thr
NM_000475.4:c.1063G>A NP_000466.2:p.Ala355Thr
NM_000475.5:c.1063G>A MANE Select NP_000466.2:p.Ala355Thr
Search 100 bp 5'
Search 100 bp 3'