Canonical Allele Identifier: CA1242198308
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531382C= , CM000664.2:g.31531382C= GRCh38
NC_000002.11:g.31756452C= , CM000664.1:g.31756452C= GRCh37
NC_000002.10:g.31609956C= NCBI36
NG_008365.1:g.54590G=

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.536G= MANE Select ENSP00000477587.1:p.Arg179=
ENST00000622030.1:c.536G= ENSP00000477587.1:p.Arg179=
NM_000348.3:c.536G= NP_000339.2:p.Arg179=
XM_011533069.1:c.314G= XP_011531371.1:p.Arg105=
XM_011533070.1:c.281G= XP_011531372.1:p.Arg94=
XM_011533071.1:c.281G= XP_011531373.1:p.Arg94=
XM_011533072.1:c.281G= XP_011531374.1:p.Arg94=
XM_011533069.2:c.314G= XP_011531371.1:p.Arg105=
XM_011533072.2:c.281G= XP_011531374.1:p.Arg94=
NM_000348.4:c.536G= MANE Select NP_000339.2:p.Arg179=