Canonical Allele Identifier: CA341535887

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737162T>A , CM000663.2:g.109737162T>A GRCh38
NC_000001.10:g.110279784T>A , CM000663.1:g.110279784T>A GRCh37
NC_000001.9:g.110081307T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.587A>T (GSTM3) MANE Select ENSP00000354357.2:p.Glu196Val
ENST00000256594.7:c.587A>T (GSTM3) ENSP00000256594.3:p.Glu196Val
ENST00000361066.6:c.587A>T (GSTM3) ENSP00000354357.2:p.Glu196Val
ENST00000429410.2:n.82+24814T>A (GSTM5)
ENST00000476321.5:n.555A>T (GSTM3)
ENST00000486823.5:n.551A>T (GSTM3)
ENST00000488824.1:n.932A>T (GSTM3)
NM_000849.4:c.587A>T (GSTM3) NP_000840.2:p.Glu196Val
NR_024537.1:n.821A>T (GSTM3)
XM_011541296.1:c.806A>T (GSTM3) XP_011539598.1:p.Glu269Val
NM_000849.5:c.587A>T (GSTM3) MANE Select NP_000840.2:p.Glu196Val
NR_024537.2:n.821A>T (GSTM3)