Canonical Allele Identifier: CA1188220547

Linked Data

dbSNP Id: rs1649230821

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737318C>T , CM000663.2:g.109737318C>T GRCh38
NC_000001.10:g.110279940C>T , CM000663.1:g.110279940C>T GRCh37
NC_000001.9:g.110081463C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.579+139G>A (GSTM3) MANE Select ENSP00000354357.2:n.579+139G>A
ENST00000256594.7:c.579+139G>A (GSTM3) ENSP00000256594.3:n.579+139G>A
ENST00000361066.6:c.579+139G>A (GSTM3) ENSP00000354357.2:n.579+139G>A
ENST00000429410.2:n.82+24970C>T (GSTM5)
ENST00000476321.5:n.399G>A (GSTM3)
ENST00000486823.5:n.543+139G>A (GSTM3)
ENST00000488824.1:n.924+139G>A (GSTM3)
NM_000849.4:c.579+139G>A (GSTM3) NP_000840.2:n.579+139G>A
NR_024537.1:n.813+139G>A (GSTM3)
XM_011541296.1:c.798+139G>A (GSTM3) XP_011539598.1:n.798+139G>A
NM_000849.5:c.579+139G>A (GSTM3) MANE Select NP_000840.2:n.579+139G>A
NR_024537.2:n.813+139G>A (GSTM3)