Canonical Allele Identifier: CA346597886

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31754401C>A (hg19) ; chr2:g.31529331C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529331C>A , CM000664.2:g.31529331C>A	GRCh38
NC_000002.11:g.31754401C>A , CM000664.1:g.31754401C>A	GRCh37
NC_000002.10:g.31607905C>A	NCBI36
NG_008365.1:g.56641G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.674G>T MANE Select	ENSP00000477587.1:p.Gly225Val
ENST00000622030.1:c.674G>T	ENSP00000477587.1:p.Gly225Val
NM_000348.3:c.674G>T	NP_000339.2:p.Gly225Val
XM_011533069.1:c.452G>T	XP_011531371.1:p.Gly151Val
XM_011533070.1:c.419G>T	XP_011531372.1:p.Gly140Val
XM_011533071.1:c.419G>T	XP_011531373.1:p.Gly140Val
XM_011533072.1:c.419G>T	XP_011531374.1:p.Gly140Val
XM_011533069.2:c.452G>T	XP_011531371.1:p.Gly151Val
XM_011533072.2:c.419G>T	XP_011531374.1:p.Gly140Val
NM_000348.4:c.674G>T MANE Select	NP_000339.2:p.Gly225Val