Canonical Allele Identifier: CA341535521

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.658G>C (GSTM3) MANE Select ENSP00000354357.2:p.Gly220Arg
ENST00000256594.7:c.658G>C (GSTM3) ENSP00000256594.3:p.Gly220Arg
ENST00000361066.6:c.658G>C (GSTM3) ENSP00000354357.2:p.Gly220Arg
ENST00000429410.2:n.82+24743C>G (GSTM5)
ENST00000476321.5:n.626G>C (GSTM3)
ENST00000486823.5:n.622G>C (GSTM3)
ENST00000488824.1:n.1003G>C (GSTM3)
NM_000849.4:c.658G>C (GSTM3) NP_000840.2:p.Gly220Arg
NR_024537.1:n.892G>C (GSTM3)
XM_011541296.1:c.877G>C (GSTM3) XP_011539598.1:p.Gly293Arg
NM_000849.5:c.658G>C (GSTM3) MANE Select NP_000840.2:p.Gly220Arg
NR_024537.2:n.892G>C (GSTM3)