Canonical Allele Identifier: CA346598563

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1665964019
• gnomAD v4: 2-31533677-A-T
• MyVariant Identifiers: chr2:g.31758747A>T (hg19) ; chr2:g.31533677A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533677A>T , CM000664.2:g.31533677A>T	GRCh38
NC_000002.11:g.31758747A>T , CM000664.1:g.31758747A>T	GRCh37
NC_000002.10:g.31612251A>T	NCBI36
NG_008365.1:g.52295T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.371T>A MANE Select	ENSP00000477587.1:p.Val124Asp
ENST00000622030.1:c.371T>A	ENSP00000477587.1:p.Val124Asp
NM_000348.3:c.371T>A	NP_000339.2:p.Val124Asp
XM_011533068.1:c.371T>A	XP_011531370.1:p.Val124Asp
XM_011533069.1:c.149T>A	XP_011531371.1:p.Val50Asp
XM_011533070.1:c.116T>A	XP_011531372.1:p.Val39Asp
XM_011533071.1:c.116T>A	XP_011531373.1:p.Val39Asp
XM_011533072.1:c.116T>A	XP_011531374.1:p.Val39Asp
XM_011533069.2:c.149T>A	XP_011531371.1:p.Val50Asp
XM_011533072.2:c.116T>A	XP_011531374.1:p.Val39Asp
NM_000348.4:c.371T>A MANE Select	NP_000339.2:p.Val124Asp