Canonical Allele Identifier: CA1139773266

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737079C= , CM000663.2:g.109737079C= GRCh38
NC_000001.10:g.110279701C= , CM000663.1:g.110279701C= GRCh37
NC_000001.9:g.110081224C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.670G= (GSTM3) MANE Select ENSP00000354357.2:p.Val224=
ENST00000256594.7:c.670G= (GSTM3) ENSP00000256594.3:p.Val224=
ENST00000361066.6:c.670G= (GSTM3) ENSP00000354357.2:p.Val224=
ENST00000429410.2:n.82+24731C= (GSTM5)
ENST00000476321.5:n.638G= (GSTM3)
ENST00000486823.5:n.634G= (GSTM3)
ENST00000488824.1:n.1015G= (GSTM3)
NM_000849.4:c.670G= (GSTM3) NP_000840.2:p.Val224=
NR_024537.1:n.904G= (GSTM3)
XM_011541296.1:c.889G= (GSTM3) XP_011539598.1:p.Val297=
NM_000849.5:c.670G= (GSTM3) MANE Select NP_000840.2:p.Val224=
NR_024537.2:n.904G= (GSTM3)