Canonical Allele Identifier: CA1188220355

Linked Data

dbSNP Id: rs1649211582

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736781C>T , CM000663.2:g.109736781C>T GRCh38
NC_000001.10:g.110279403C>T , CM000663.1:g.110279403C>T GRCh37
NC_000001.9:g.110080926C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*290G>A (GSTM3) MANE Select ENSP00000354357.2:n.*290G>A
ENST00000256594.7:c.*290G>A (GSTM3) ENSP00000256594.3:n.*290G>A
ENST00000361066.6:c.*290G>A (GSTM3) ENSP00000354357.2:n.*290G>A
ENST00000429410.2:n.82+24433C>T (GSTM5)
NM_000849.4:c.*290G>A (GSTM3) NP_000840.2:n.*290G>A
NR_024537.1:n.1202G>A (GSTM3)
NM_000849.5:c.*290G>A (GSTM3) MANE Select NP_000840.2:n.*290G>A
NR_024537.2:n.1202G>A (GSTM3)