Canonical Allele Identifier: CA1242214596

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1666752962

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567419A>G , CM000664.2:g.31567419A>G	GRCh38
NC_000002.11:g.31792489A>G , CM000664.1:g.31792489A>G	GRCh37
NC_000002.10:g.31645993A>G	NCBI36
NG_008365.1:g.18553T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13201T>C MANE Select	ENSP00000477587.1:n.281+13201T>C
ENST00000622030.1:c.281+13201T>C	ENSP00000477587.1:n.281+13201T>C
NM_000348.3:c.281+13201T>C	NP_000339.2:n.281+13201T>C
XM_011533068.1:c.281+13201T>C	XP_011531370.1:n.281+13201T>C
XM_011533070.1:c.27-33653T>C	XP_011531372.1:n.27-33653T>C
XM_011533071.1:c.27-33653T>C	XP_011531373.1:n.27-33653T>C
XM_011533072.1:c.27-33653T>C	XP_011531374.1:n.27-33653T>C
XM_011533072.2:c.27-33653T>C	XP_011531374.1:n.27-33653T>C
NM_000348.4:c.281+13201T>C MANE Select	NP_000339.2:n.281+13201T>C