Canonical Allele Identifier: CA1242214676
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567542A= , CM000664.2:g.31567542A= GRCh38
NC_000002.11:g.31792612A= , CM000664.1:g.31792612A= GRCh37
NC_000002.10:g.31646116A= NCBI36
NG_008365.1:g.18430T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13078T= MANE Select ENSP00000477587.1:n.281+13078T=
ENST00000622030.1:c.281+13078T= ENSP00000477587.1:n.281+13078T=
NM_000348.3:c.281+13078T= NP_000339.2:n.281+13078T=
XM_011533068.1:c.281+13078T= XP_011531370.1:n.281+13078T=
XM_011533070.1:c.27-33776T= XP_011531372.1:n.27-33776T=
XM_011533071.1:c.27-33776T= XP_011531373.1:n.27-33776T=
XM_011533072.1:c.27-33776T= XP_011531374.1:n.27-33776T=
XM_011533072.2:c.27-33776T= XP_011531374.1:n.27-33776T=
NM_000348.4:c.281+13078T= MANE Select NP_000339.2:n.281+13078T=