Canonical Allele Identifier: CA1242195092
Gene: SRD5A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31523858A= , CM000664.2:g.31523858A= GRCh38
NC_000002.11:g.31748928A= , CM000664.1:g.31748928A= GRCh37
NC_000002.10:g.31602432A= NCBI36
NG_008365.1:g.62114T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.*2338T= MANE Select ENSP00000477587.1:n.*2338T=
ENST00000622030.1:c.*2338T= ENSP00000477587.1:n.*2338T=
XM_011533069.1:c.*2338T= XP_011531371.1:n.*2338T=
XM_011533070.1:c.*2338T= XP_011531372.1:n.*2338T=
XM_011533071.1:c.*2338T= XP_011531373.1:n.*2338T=
XM_011533072.1:c.*2338T= XP_011531374.1:n.*2338T=
XM_011533069.2:c.*2338T= XP_011531371.1:n.*2338T=
XM_011533072.2:c.*2338T= XP_011531374.1:n.*2338T=
NM_000348.4:c.*2338T= MANE Select NP_000339.2:n.*2338T=
Search 100 bp 5'
Search 100 bp 3'