Canonical Allele Identifier: CA341535532

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737093C>G , CM000663.2:g.109737093C>G GRCh38
NC_000001.10:g.110279715C>G , CM000663.1:g.110279715C>G GRCh37
NC_000001.9:g.110081238C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.656G>C (GSTM3) MANE Select ENSP00000354357.2:p.Trp219Ser
ENST00000256594.7:c.656G>C (GSTM3) ENSP00000256594.3:p.Trp219Ser
ENST00000361066.6:c.656G>C (GSTM3) ENSP00000354357.2:p.Trp219Ser
ENST00000429410.2:n.82+24745C>G (GSTM5)
ENST00000476321.5:n.624G>C (GSTM3)
ENST00000486823.5:n.620G>C (GSTM3)
ENST00000488824.1:n.1001G>C (GSTM3)
NM_000849.4:c.656G>C (GSTM3) NP_000840.2:p.Trp219Ser
NR_024537.1:n.890G>C (GSTM3)
XM_011541296.1:c.875G>C (GSTM3) XP_011539598.1:p.Trp292Ser
NM_000849.5:c.656G>C (GSTM3) MANE Select NP_000840.2:p.Trp219Ser
NR_024537.2:n.890G>C (GSTM3)