Canonical Allele Identifier: CA346598316
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531442A>G , CM000664.2:g.31531442A>G GRCh38
NC_000002.11:g.31756512A>G , CM000664.1:g.31756512A>G GRCh37
NC_000002.10:g.31610016A>G NCBI36
NG_008365.1:g.54530T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.476T>C MANE Select ENSP00000477587.1:p.Ile159Thr
ENST00000622030.1:c.476T>C ENSP00000477587.1:p.Ile159Thr
NM_000348.3:c.476T>C NP_000339.2:p.Ile159Thr
XM_011533069.1:c.254T>C XP_011531371.1:p.Ile85Thr
XM_011533070.1:c.221T>C XP_011531372.1:p.Ile74Thr
XM_011533071.1:c.221T>C XP_011531373.1:p.Ile74Thr
XM_011533072.1:c.221T>C XP_011531374.1:p.Ile74Thr
XM_011533069.2:c.254T>C XP_011531371.1:p.Ile85Thr
XM_011533072.2:c.221T>C XP_011531374.1:p.Ile74Thr
NM_000348.4:c.476T>C MANE Select NP_000339.2:p.Ile159Thr