Canonical Allele Identifier: CA1242197455
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529498A= , CM000664.2:g.31529498A= GRCh38
NC_000002.11:g.31754568A= , CM000664.1:g.31754568A= GRCh37
NC_000002.10:g.31608072A= NCBI36
NG_008365.1:g.56474T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.548-41T= MANE Select ENSP00000477587.1:n.548-41T=
ENST00000622030.1:c.548-41T= ENSP00000477587.1:n.548-41T=
NM_000348.3:c.548-41T= NP_000339.2:n.548-41T=
XM_011533069.1:c.326-41T= XP_011531371.1:n.326-41T=
XM_011533070.1:c.293-41T= XP_011531372.1:n.293-41T=
XM_011533071.1:c.293-41T= XP_011531373.1:n.293-41T=
XM_011533072.1:c.293-41T= XP_011531374.1:n.293-41T=
XM_011533069.2:c.326-41T= XP_011531371.1:n.326-41T=
XM_011533072.2:c.293-41T= XP_011531374.1:n.293-41T=
NM_000348.4:c.548-41T= MANE Select NP_000339.2:n.548-41T=