Canonical Allele Identifier: CA1143429299

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737140C= , CM000663.2:g.109737140C= GRCh38
NC_000001.10:g.110279762C= , CM000663.1:g.110279762C= GRCh37
NC_000001.9:g.110081285C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.609G= (GSTM3) MANE Select ENSP00000354357.2:p.Gln203=
ENST00000256594.7:c.609G= (GSTM3) ENSP00000256594.3:p.Gln203=
ENST00000361066.6:c.609G= (GSTM3) ENSP00000354357.2:p.Gln203=
ENST00000429410.2:n.82+24792C= (GSTM5)
ENST00000476321.5:n.577G= (GSTM3)
ENST00000486823.5:n.573G= (GSTM3)
ENST00000488824.1:n.954G= (GSTM3)
NM_000849.4:c.609G= (GSTM3) NP_000840.2:p.Gln203=
NR_024537.1:n.843G= (GSTM3)
XM_011541296.1:c.828G= (GSTM3) XP_011539598.1:p.Gln276=
NM_000849.5:c.609G= (GSTM3) MANE Select NP_000840.2:p.Gln203=
NR_024537.2:n.843G= (GSTM3)