Canonical Allele Identifier: CA1188220451

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737091C= , CM000663.2:g.109737091C= GRCh38
NC_000001.10:g.110279713C= , CM000663.1:g.110279713C= GRCh37
NC_000001.9:g.110081236C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.658G= (GSTM3) MANE Select ENSP00000354357.2:p.Gly220=
ENST00000256594.7:c.658G= (GSTM3) ENSP00000256594.3:p.Gly220=
ENST00000361066.6:c.658G= (GSTM3) ENSP00000354357.2:p.Gly220=
ENST00000429410.2:n.82+24743C= (GSTM5)
ENST00000476321.5:n.626G= (GSTM3)
ENST00000486823.5:n.622G= (GSTM3)
ENST00000488824.1:n.1003G= (GSTM3)
NM_000849.4:c.658G= (GSTM3) NP_000840.2:p.Gly220=
NR_024537.1:n.892G= (GSTM3)
XM_011541296.1:c.877G= (GSTM3) XP_011539598.1:p.Gly293=
NM_000849.5:c.658G= (GSTM3) MANE Select NP_000840.2:p.Gly220=
NR_024537.2:n.892G= (GSTM3)