Canonical Allele Identifier: CA341535431

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737074G>C , CM000663.2:g.109737074G>C GRCh38
NC_000001.10:g.110279696G>C , CM000663.1:g.110279696G>C GRCh37
NC_000001.9:g.110081219G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.675C>G (GSTM3) MANE Select ENSP00000354357.2:p.Cys225Trp
ENST00000256594.7:c.675C>G (GSTM3) ENSP00000256594.3:p.Cys225Trp
ENST00000361066.6:c.675C>G (GSTM3) ENSP00000354357.2:p.Cys225Trp
ENST00000429410.2:n.82+24726G>C (GSTM5)
ENST00000476321.5:n.643C>G (GSTM3)
ENST00000486823.5:n.639C>G (GSTM3)
ENST00000488824.1:n.1020C>G (GSTM3)
NM_000849.4:c.675C>G (GSTM3) NP_000840.2:p.Cys225Trp
NR_024537.1:n.909C>G (GSTM3)
XM_011541296.1:c.894C>G (GSTM3) XP_011539598.1:p.Cys298Trp
NM_000849.5:c.675C>G (GSTM3) MANE Select NP_000840.2:p.Cys225Trp
NR_024537.2:n.909C>G (GSTM3)