Canonical Allele Identifier: CA1242215067
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31568340C= , CM000664.2:g.31568340C= GRCh38
NC_000002.11:g.31793410C= , CM000664.1:g.31793410C= GRCh37
NC_000002.10:g.31646914C= NCBI36
NG_008365.1:g.17632G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+12280G= MANE Select ENSP00000477587.1:n.281+12280G=
ENST00000622030.1:c.281+12280G= ENSP00000477587.1:n.281+12280G=
NM_000348.3:c.281+12280G= NP_000339.2:n.281+12280G=
XM_011533068.1:c.281+12280G= XP_011531370.1:n.281+12280G=
XM_011533070.1:c.27-34574G= XP_011531372.1:n.27-34574G=
XM_011533071.1:c.27-34574G= XP_011531373.1:n.27-34574G=
XM_011533072.1:c.27-34574G= XP_011531374.1:n.27-34574G=
XM_011533072.2:c.27-34574G= XP_011531374.1:n.27-34574G=
NM_000348.4:c.281+12280G= MANE Select NP_000339.2:n.281+12280G=