Canonical Allele Identifier: CA994810

Linked Data

dbSNP Id: rs756172132

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737037G>T , CM000663.2:g.109737037G>T GRCh38
NC_000001.10:g.110279659G>T , CM000663.1:g.110279659G>T GRCh37
NC_000001.9:g.110081182G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*34C>A (GSTM3) MANE Select ENSP00000354357.2:n.*34C>A
ENST00000256594.7:c.*34C>A (GSTM3) ENSP00000256594.3:n.*34C>A
ENST00000361066.6:c.*34C>A (GSTM3) ENSP00000354357.2:n.*34C>A
ENST00000429410.2:n.82+24689G>T (GSTM5)
ENST00000476321.5:n.680C>A (GSTM3)
ENST00000486823.5:n.676C>A (GSTM3)
ENST00000488824.1:n.1057C>A (GSTM3)
NM_000849.4:c.*34C>A (GSTM3) NP_000840.2:n.*34C>A
NR_024537.1:n.946C>A (GSTM3)
XM_011541296.1:c.*34C>A (GSTM3) XP_011539598.1:n.*34C>A
NM_000849.5:c.*34C>A (GSTM3) MANE Select NP_000840.2:n.*34C>A
NR_024537.2:n.946C>A (GSTM3)