Canonical Allele Identifier: CA1242199392
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533793G= , CM000664.2:g.31533793G= GRCh38
NC_000002.11:g.31758863G= , CM000664.1:g.31758863G= GRCh37
NC_000002.10:g.31612367G= NCBI36
NG_008365.1:g.52179C=

Transcript Alleles

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