Canonical Allele Identifier: CA341535722

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737129A>C , CM000663.2:g.109737129A>C GRCh38
NC_000001.10:g.110279751A>C , CM000663.1:g.110279751A>C GRCh37
NC_000001.9:g.110081274A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.620T>G (GSTM3) MANE Select ENSP00000354357.2:p.Phe207Cys
ENST00000256594.7:c.620T>G (GSTM3) ENSP00000256594.3:p.Phe207Cys
ENST00000361066.6:c.620T>G (GSTM3) ENSP00000354357.2:p.Phe207Cys
ENST00000429410.2:n.82+24781A>C (GSTM5)
ENST00000476321.5:n.588T>G (GSTM3)
ENST00000486823.5:n.584T>G (GSTM3)
ENST00000488824.1:n.965T>G (GSTM3)
NM_000849.4:c.620T>G (GSTM3) NP_000840.2:p.Phe207Cys
NR_024537.1:n.854T>G (GSTM3)
XM_011541296.1:c.839T>G (GSTM3) XP_011539598.1:p.Phe280Cys
NM_000849.5:c.620T>G (GSTM3) MANE Select NP_000840.2:p.Phe207Cys
NR_024537.2:n.854T>G (GSTM3)