Canonical Allele Identifier: CA1242199464

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1665971822

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533962C>T , CM000664.2:g.31533962C>T	GRCh38
NC_000002.11:g.31759032C>T , CM000664.1:g.31759032C>T	GRCh37
NC_000002.10:g.31612536C>T	NCBI36
NG_008365.1:g.52010G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.282-196G>A MANE Select	ENSP00000477587.1:n.282-196G>A
ENST00000622030.1:c.282-196G>A	ENSP00000477587.1:n.282-196G>A
NM_000348.3:c.282-196G>A	NP_000339.2:n.282-196G>A
XM_011533068.1:c.282-196G>A	XP_011531370.1:n.282-196G>A
XM_011533069.1:c.60-196G>A	XP_011531371.1:n.60-196G>A
XM_011533070.1:c.27-196G>A	XP_011531372.1:n.27-196G>A
XM_011533071.1:c.27-196G>A	XP_011531373.1:n.27-196G>A
XM_011533072.1:c.27-196G>A	XP_011531374.1:n.27-196G>A
XM_011533069.2:c.60-196G>A	XP_011531371.1:n.60-196G>A
XM_011533072.2:c.27-196G>A	XP_011531374.1:n.27-196G>A
NM_000348.4:c.282-196G>A MANE Select	NP_000339.2:n.282-196G>A