Canonical Allele Identifier: CA327974124

Gene: NR0B1

Linked Data

• dbSNP Id: rs866647367
• MyVariant Identifiers: chrX:g.30322807G>A (hg19) ; chrX:g.30304690G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30304690G>A , CM000685.2:g.30304690G>A	GRCh38
NC_000023.10:g.30322807G>A , CM000685.1:g.30322807G>A	GRCh37
NC_000023.9:g.30232728G>A	NCBI36
NG_009814.1:g.9689C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378970.5:c.1302C>T MANE Select	ENSP00000368253.4:p.Phe434=
ENST00000378970.4:c.1302C>T	ENSP00000368253.4:p.Phe434=
NM_000475.4:c.1302C>T	NP_000466.2:p.Phe434=
NM_000475.5:c.1302C>T MANE Select	NP_000466.2:p.Phe434=