Canonical Allele Identifier: CA341535763

Linked Data

dbSNP Id: rs1459134925

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737136C>A , CM000663.2:g.109737136C>A GRCh38
NC_000001.10:g.110279758C>A , CM000663.1:g.110279758C>A GRCh37
NC_000001.9:g.110081281C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.613G>T (GSTM3) MANE Select ENSP00000354357.2:p.Asp205Tyr
ENST00000256594.7:c.613G>T (GSTM3) ENSP00000256594.3:p.Asp205Tyr
ENST00000361066.6:c.613G>T (GSTM3) ENSP00000354357.2:p.Asp205Tyr
ENST00000429410.2:n.82+24788C>A (GSTM5)
ENST00000476321.5:n.581G>T (GSTM3)
ENST00000486823.5:n.577G>T (GSTM3)
ENST00000488824.1:n.958G>T (GSTM3)
NM_000849.4:c.613G>T (GSTM3) NP_000840.2:p.Asp205Tyr
NR_024537.1:n.847G>T (GSTM3)
XM_011541296.1:c.832G>T (GSTM3) XP_011539598.1:p.Asp278Tyr
NM_000849.5:c.613G>T (GSTM3) MANE Select NP_000840.2:p.Asp205Tyr
NR_024537.2:n.847G>T (GSTM3)