Canonical Allele Identifier: CA419374170

Linked Data

dbSNP Id: rs1406669726

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736978C>T , CM000663.2:g.109736978C>T GRCh38
NC_000001.10:g.110279600C>T , CM000663.1:g.110279600C>T GRCh37
NC_000001.9:g.110081123C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*93G>A (GSTM3) MANE Select ENSP00000354357.2:n.*93G>A
ENST00000256594.7:c.*93G>A (GSTM3) ENSP00000256594.3:n.*93G>A
ENST00000361066.6:c.*93G>A (GSTM3) ENSP00000354357.2:n.*93G>A
ENST00000429410.2:n.82+24630C>T (GSTM5)
ENST00000476321.5:n.739G>A (GSTM3)
ENST00000486823.5:n.735G>A (GSTM3)
ENST00000488824.1:n.1116G>A (GSTM3)
NM_000849.4:c.*93G>A (GSTM3) NP_000840.2:n.*93G>A
NR_024537.1:n.1005G>A (GSTM3)
XM_011541296.1:c.*93G>A (GSTM3) XP_011539598.1:n.*93G>A
NM_000849.5:c.*93G>A (GSTM3) MANE Select NP_000840.2:n.*93G>A
NR_024537.2:n.1005G>A (GSTM3)