Canonical Allele Identifier: CA1242195123
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31523958T= , CM000664.2:g.31523958T= GRCh38
NC_000002.11:g.31749028T= , CM000664.1:g.31749028T= GRCh37
NC_000002.10:g.31602532T= NCBI36
NG_008365.1:g.62014A=

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.*2238A= MANE Select ENSP00000477587.1:n.*2238A=
ENST00000622030.1:c.*2238A= ENSP00000477587.1:n.*2238A=
XM_011533069.1:c.*2238A= XP_011531371.1:n.*2238A=
XM_011533070.1:c.*2238A= XP_011531372.1:n.*2238A=
XM_011533071.1:c.*2238A= XP_011531373.1:n.*2238A=
XM_011533072.1:c.*2238A= XP_011531374.1:n.*2238A=
XM_011533069.2:c.*2238A= XP_011531371.1:n.*2238A=
XM_011533072.2:c.*2238A= XP_011531374.1:n.*2238A=
NM_000348.4:c.*2238A= MANE Select NP_000339.2:n.*2238A=