Canonical Allele Identifier: CA1188220400

Linked Data

dbSNP Id: rs1649213877

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736891A>G , CM000663.2:g.109736891A>G GRCh38
NC_000001.10:g.110279513A>G , CM000663.1:g.110279513A>G GRCh37
NC_000001.9:g.110081036A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*180T>C (GSTM3) MANE Select ENSP00000354357.2:n.*180T>C
ENST00000256594.7:c.*180T>C (GSTM3) ENSP00000256594.3:n.*180T>C
ENST00000361066.6:c.*180T>C (GSTM3) ENSP00000354357.2:n.*180T>C
ENST00000429410.2:n.82+24543A>G (GSTM5)
NM_000849.4:c.*180T>C (GSTM3) NP_000840.2:n.*180T>C
NR_024537.1:n.1092T>C (GSTM3)
NM_000849.5:c.*180T>C (GSTM3) MANE Select NP_000840.2:n.*180T>C
NR_024537.2:n.1092T>C (GSTM3)