Canonical Allele Identifier: CA1242197307
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529193C= , CM000664.2:g.31529193C= GRCh38
NC_000002.11:g.31754263C= , CM000664.1:g.31754263C= GRCh37
NC_000002.10:g.31607767C= NCBI36
NG_008365.1:g.56779G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.698+114G= MANE Select ENSP00000477587.1:n.698+114G=
ENST00000622030.1:c.698+114G= ENSP00000477587.1:n.698+114G=
NM_000348.3:c.698+114G= NP_000339.2:n.698+114G=
XM_011533069.1:c.476+114G= XP_011531371.1:n.476+114G=
XM_011533070.1:c.443+114G= XP_011531372.1:n.443+114G=
XM_011533071.1:c.443+114G= XP_011531373.1:n.443+114G=
XM_011533072.1:c.443+114G= XP_011531374.1:n.443+114G=
XM_011533069.2:c.476+114G= XP_011531371.1:n.476+114G=
XM_011533072.2:c.443+114G= XP_011531374.1:n.443+114G=
NM_000348.4:c.698+114G= MANE Select NP_000339.2:n.698+114G=