Canonical Allele Identifier: CA1005674674

Linked Data

dbSNP Id: rs1557978799

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736782T>G , CM000663.2:g.109736782T>G GRCh38
NC_000001.10:g.110279404T>G , CM000663.1:g.110279404T>G GRCh37
NC_000001.9:g.110080927T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*289A>C (GSTM3) MANE Select ENSP00000354357.2:n.*289A>C
ENST00000256594.7:c.*289A>C (GSTM3) ENSP00000256594.3:n.*289A>C
ENST00000361066.6:c.*289A>C (GSTM3) ENSP00000354357.2:n.*289A>C
ENST00000429410.2:n.82+24434T>G (GSTM5)
NM_000849.4:c.*289A>C (GSTM3) NP_000840.2:n.*289A>C
NR_024537.1:n.1201A>C (GSTM3)
NM_000849.5:c.*289A>C (GSTM3) MANE Select NP_000840.2:n.*289A>C
NR_024537.2:n.1201A>C (GSTM3)