Canonical Allele Identifier: CA341535920

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737166A>T , CM000663.2:g.109737166A>T GRCh38
NC_000001.10:g.110279788A>T , CM000663.1:g.110279788A>T GRCh37
NC_000001.9:g.110081311A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.583T>A (GSTM3) MANE Select ENSP00000354357.2:p.Leu195Met
ENST00000256594.7:c.583T>A (GSTM3) ENSP00000256594.3:p.Leu195Met
ENST00000361066.6:c.583T>A (GSTM3) ENSP00000354357.2:p.Leu195Met
ENST00000429410.2:n.82+24818A>T (GSTM5)
ENST00000476321.5:n.551T>A (GSTM3)
ENST00000486823.5:n.547T>A (GSTM3)
ENST00000488824.1:n.928T>A (GSTM3)
NM_000849.4:c.583T>A (GSTM3) NP_000840.2:p.Leu195Met
NR_024537.1:n.817T>A (GSTM3)
XM_011541296.1:c.802T>A (GSTM3) XP_011539598.1:p.Leu268Met
NM_000849.5:c.583T>A (GSTM3) MANE Select NP_000840.2:p.Leu195Met
NR_024537.2:n.817T>A (GSTM3)