Canonical Allele Identifier: CA1146878729

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737155G= , CM000663.2:g.109737155G= GRCh38
NC_000001.10:g.110279777G= , CM000663.1:g.110279777G= GRCh37
NC_000001.9:g.110081300G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.594C= (GSTM3) MANE Select ENSP00000354357.2:p.Ile198=
ENST00000256594.7:c.594C= (GSTM3) ENSP00000256594.3:p.Ile198=
ENST00000361066.6:c.594C= (GSTM3) ENSP00000354357.2:p.Ile198=
ENST00000429410.2:n.82+24807G= (GSTM5)
ENST00000476321.5:n.562C= (GSTM3)
ENST00000486823.5:n.558C= (GSTM3)
ENST00000488824.1:n.939C= (GSTM3)
NM_000849.4:c.594C= (GSTM3) NP_000840.2:p.Ile198=
NR_024537.1:n.828C= (GSTM3)
XM_011541296.1:c.813C= (GSTM3) XP_011539598.1:p.Ile271=
NM_000849.5:c.594C= (GSTM3) MANE Select NP_000840.2:p.Ile198=
NR_024537.2:n.828C= (GSTM3)