Canonical Allele Identifier: CA1242197351
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529286C= , CM000664.2:g.31529286C= GRCh38
NC_000002.11:g.31754356C= , CM000664.1:g.31754356C= GRCh37
NC_000002.10:g.31607860C= NCBI36
NG_008365.1:g.56686G=

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.698+21G= MANE Select ENSP00000477587.1:n.698+21G=
ENST00000622030.1:c.698+21G= ENSP00000477587.1:n.698+21G=
NM_000348.3:c.698+21G= NP_000339.2:n.698+21G=
XM_011533069.1:c.476+21G= XP_011531371.1:n.476+21G=
XM_011533070.1:c.443+21G= XP_011531372.1:n.443+21G=
XM_011533071.1:c.443+21G= XP_011531373.1:n.443+21G=
XM_011533072.1:c.443+21G= XP_011531374.1:n.443+21G=
XM_011533069.2:c.476+21G= XP_011531371.1:n.476+21G=
XM_011533072.2:c.443+21G= XP_011531374.1:n.443+21G=
NM_000348.4:c.698+21G= MANE Select NP_000339.2:n.698+21G=