Canonical Allele Identifier: CA425567470
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529414C>T , CM000664.2:g.31529414C>T GRCh38
NC_000002.11:g.31754484C>T , CM000664.1:g.31754484C>T GRCh37
NC_000002.10:g.31607988C>T NCBI36
NG_008365.1:g.56558G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.591G>A MANE Select ENSP00000477587.1:p.Glu197=
ENST00000622030.1:c.591G>A ENSP00000477587.1:p.Glu197=
NM_000348.3:c.591G>A NP_000339.2:p.Glu197=
XM_011533069.1:c.369G>A XP_011531371.1:p.Glu123=
XM_011533070.1:c.336G>A XP_011531372.1:p.Glu112=
XM_011533071.1:c.336G>A XP_011531373.1:p.Glu112=
XM_011533072.1:c.336G>A XP_011531374.1:p.Glu112=
XM_011533069.2:c.369G>A XP_011531371.1:p.Glu123=
XM_011533072.2:c.336G>A XP_011531374.1:p.Glu112=
NM_000348.4:c.591G>A MANE Select NP_000339.2:p.Glu197=