Canonical Allele Identifier: CA1242214665
Gene: SRD5A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567507C= , CM000664.2:g.31567507C= GRCh38
NC_000002.11:g.31792577C= , CM000664.1:g.31792577C= GRCh37
NC_000002.10:g.31646081C= NCBI36
NG_008365.1:g.18465G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13113G= MANE Select ENSP00000477587.1:n.281+13113G=
ENST00000622030.1:c.281+13113G= ENSP00000477587.1:n.281+13113G=
NM_000348.3:c.281+13113G= NP_000339.2:n.281+13113G=
XM_011533068.1:c.281+13113G= XP_011531370.1:n.281+13113G=
XM_011533070.1:c.27-33741G= XP_011531372.1:n.27-33741G=
XM_011533071.1:c.27-33741G= XP_011531373.1:n.27-33741G=
XM_011533072.1:c.27-33741G= XP_011531374.1:n.27-33741G=
XM_011533072.2:c.27-33741G= XP_011531374.1:n.27-33741G=
NM_000348.4:c.281+13113G= MANE Select NP_000339.2:n.281+13113G=
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