Canonical Allele Identifier: CA346598187
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531385T>A , CM000664.2:g.31531385T>A GRCh38
NC_000002.11:g.31756455T>A , CM000664.1:g.31756455T>A GRCh37
NC_000002.10:g.31609959T>A NCBI36
NG_008365.1:g.54587A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.533A>T MANE Select ENSP00000477587.1:p.Tyr178Phe
ENST00000622030.1:c.533A>T ENSP00000477587.1:p.Tyr178Phe
NM_000348.3:c.533A>T NP_000339.2:p.Tyr178Phe
XM_011533069.1:c.311A>T XP_011531371.1:p.Tyr104Phe
XM_011533070.1:c.278A>T XP_011531372.1:p.Tyr93Phe
XM_011533071.1:c.278A>T XP_011531373.1:p.Tyr93Phe
XM_011533072.1:c.278A>T XP_011531374.1:p.Tyr93Phe
XM_011533069.2:c.311A>T XP_011531371.1:p.Tyr104Phe
XM_011533072.2:c.278A>T XP_011531374.1:p.Tyr93Phe
NM_000348.4:c.533A>T MANE Select NP_000339.2:p.Tyr178Phe