Canonical Allele Identifier: CA346597988
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529380A>T , CM000664.2:g.31529380A>T GRCh38
NC_000002.11:g.31754450A>T , CM000664.1:g.31754450A>T GRCh37
NC_000002.10:g.31607954A>T NCBI36
NG_008365.1:g.56592T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.625T>A MANE Select ENSP00000477587.1:p.Trp209Arg
ENST00000622030.1:c.625T>A ENSP00000477587.1:p.Trp209Arg
NM_000348.3:c.625T>A NP_000339.2:p.Trp209Arg
XM_011533069.1:c.403T>A XP_011531371.1:p.Trp135Arg
XM_011533070.1:c.370T>A XP_011531372.1:p.Trp124Arg
XM_011533071.1:c.370T>A XP_011531373.1:p.Trp124Arg
XM_011533072.1:c.370T>A XP_011531374.1:p.Trp124Arg
XM_011533069.2:c.403T>A XP_011531371.1:p.Trp135Arg
XM_011533072.2:c.370T>A XP_011531374.1:p.Trp124Arg
NM_000348.4:c.625T>A MANE Select NP_000339.2:p.Trp209Arg