Canonical Allele Identifier: CA341535541

Linked Data

dbSNP Id: rs1570662534

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737094A>T , CM000663.2:g.109737094A>T GRCh38
NC_000001.10:g.110279716A>T , CM000663.1:g.110279716A>T GRCh37
NC_000001.9:g.110081239A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.655T>A (GSTM3) MANE Select ENSP00000354357.2:p.Trp219Arg
ENST00000256594.7:c.655T>A (GSTM3) ENSP00000256594.3:p.Trp219Arg
ENST00000361066.6:c.655T>A (GSTM3) ENSP00000354357.2:p.Trp219Arg
ENST00000429410.2:n.82+24746A>T (GSTM5)
ENST00000476321.5:n.623T>A (GSTM3)
ENST00000486823.5:n.619T>A (GSTM3)
ENST00000488824.1:n.1000T>A (GSTM3)
NM_000849.4:c.655T>A (GSTM3) NP_000840.2:p.Trp219Arg
NR_024537.1:n.889T>A (GSTM3)
XM_011541296.1:c.874T>A (GSTM3) XP_011539598.1:p.Trp292Arg
NM_000849.5:c.655T>A (GSTM3) MANE Select NP_000840.2:p.Trp219Arg
NR_024537.2:n.889T>A (GSTM3)