Canonical Allele Identifier: CA346598571

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31758751C>G (hg19) ; chr2:g.31533681C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533681C>G , CM000664.2:g.31533681C>G	GRCh38
NC_000002.11:g.31758751C>G , CM000664.1:g.31758751C>G	GRCh37
NC_000002.10:g.31612255C>G	NCBI36
NG_008365.1:g.52291G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.367G>C MANE Select	ENSP00000477587.1:p.Gly123Arg
ENST00000622030.1:c.367G>C	ENSP00000477587.1:p.Gly123Arg
NM_000348.3:c.367G>C	NP_000339.2:p.Gly123Arg
XM_011533068.1:c.367G>C	XP_011531370.1:p.Gly123Arg
XM_011533069.1:c.145G>C	XP_011531371.1:p.Gly49Arg
XM_011533070.1:c.112G>C	XP_011531372.1:p.Gly38Arg
XM_011533071.1:c.112G>C	XP_011531373.1:p.Gly38Arg
XM_011533072.1:c.112G>C	XP_011531374.1:p.Gly38Arg
XM_011533069.2:c.145G>C	XP_011531371.1:p.Gly49Arg
XM_011533072.2:c.112G>C	XP_011531374.1:p.Gly38Arg
NM_000348.4:c.367G>C MANE Select	NP_000339.2:p.Gly123Arg