Canonical Allele Identifier: CA341535708

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737125G>T , CM000663.2:g.109737125G>T GRCh38
NC_000001.10:g.110279747G>T , CM000663.1:g.110279747G>T GRCh37
NC_000001.9:g.110081270G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.624C>A (GSTM3) MANE Select ENSP00000354357.2:p.Cys208Ter
ENST00000256594.7:c.624C>A (GSTM3) ENSP00000256594.3:p.Cys208Ter
ENST00000361066.6:c.624C>A (GSTM3) ENSP00000354357.2:p.Cys208Ter
ENST00000429410.2:n.82+24777G>T (GSTM5)
ENST00000476321.5:n.592C>A (GSTM3)
ENST00000486823.5:n.588C>A (GSTM3)
ENST00000488824.1:n.969C>A (GSTM3)
NM_000849.4:c.624C>A (GSTM3) NP_000840.2:p.Cys208Ter
NR_024537.1:n.858C>A (GSTM3)
XM_011541296.1:c.843C>A (GSTM3) XP_011539598.1:p.Cys281Ter
NM_000849.5:c.624C>A (GSTM3) MANE Select NP_000840.2:p.Cys208Ter
NR_024537.2:n.858C>A (GSTM3)