Canonical Allele Identifier: CA425568479

Gene: SRD5A2

Linked Data

• gnomAD v4: 2-31533736-C-A
• MyVariant Identifiers: chr2:g.31758806C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533736C>A , CM000664.2:g.31533736C>A	GRCh38
NC_000002.11:g.31758806C>A , CM000664.1:g.31758806C>A	GRCh37
NC_000002.10:g.31612310C>A	NCBI36
NG_008365.1:g.52236G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.312G>T MANE Select	ENSP00000477587.1:p.Gly104=
ENST00000622030.1:c.312G>T	ENSP00000477587.1:p.Gly104=
NM_000348.3:c.312G>T	NP_000339.2:p.Gly104=
XM_011533068.1:c.312G>T	XP_011531370.1:p.Gly104=
XM_011533069.1:c.90G>T	XP_011531371.1:p.Gly30=
XM_011533070.1:c.57G>T	XP_011531372.1:p.Gly19=
XM_011533071.1:c.57G>T	XP_011531373.1:p.Gly19=
XM_011533072.1:c.57G>T	XP_011531374.1:p.Gly19=
XM_011533069.2:c.90G>T	XP_011531371.1:p.Gly30=
XM_011533072.2:c.57G>T	XP_011531374.1:p.Gly19=
NM_000348.4:c.312G>T MANE Select	NP_000339.2:p.Gly104=