Canonical Allele Identifier: CA1242195968
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31526274G= , CM000664.2:g.31526274G= GRCh38
NC_000002.11:g.31751344G= , CM000664.1:g.31751344G= GRCh37
NC_000002.10:g.31604848G= NCBI36
NG_008365.1:g.59698C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.699-12C= MANE Select ENSP00000477587.1:n.699-12C=
ENST00000622030.1:c.699-12C= ENSP00000477587.1:n.699-12C=
NM_000348.3:c.699-12C= NP_000339.2:n.699-12C=
XM_011533069.1:c.477-12C= XP_011531371.1:n.477-12C=
XM_011533070.1:c.444-12C= XP_011531372.1:n.444-12C=
XM_011533071.1:c.444-12C= XP_011531373.1:n.444-12C=
XM_011533072.1:c.444-12C= XP_011531374.1:n.444-12C=
XM_011533069.2:c.477-12C= XP_011531371.1:n.477-12C=
XM_011533072.2:c.444-12C= XP_011531374.1:n.444-12C=
NM_000348.4:c.699-12C= MANE Select NP_000339.2:n.699-12C=