Canonical Allele Identifier: CA1188220468

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.620T= (GSTM3) MANE Select ENSP00000354357.2:p.Phe207=
ENST00000256594.7:c.620T= (GSTM3) ENSP00000256594.3:p.Phe207=
ENST00000361066.6:c.620T= (GSTM3) ENSP00000354357.2:p.Phe207=
ENST00000429410.2:n.82+24781A= (GSTM5)
ENST00000476321.5:n.588T= (GSTM3)
ENST00000486823.5:n.584T= (GSTM3)
ENST00000488824.1:n.965T= (GSTM3)
NM_000849.4:c.620T= (GSTM3) NP_000840.2:p.Phe207=
NR_024537.1:n.854T= (GSTM3)
XM_011541296.1:c.839T= (GSTM3) XP_011539598.1:p.Phe280=
NM_000849.5:c.620T= (GSTM3) MANE Select NP_000840.2:p.Phe207=
NR_024537.2:n.854T= (GSTM3)