Canonical Allele Identifier: CA2646987398

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736887A>G , CM000663.2:g.109736887A>G GRCh38
NC_000001.10:g.110279509A>G , CM000663.1:g.110279509A>G GRCh37
NC_000001.9:g.110081032A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*184T>C (GSTM3) MANE Select ENSP00000354357.2:n.*184T>C
ENST00000256594.7:c.*184T>C (GSTM3) ENSP00000256594.3:n.*184T>C
ENST00000361066.6:c.*184T>C (GSTM3) ENSP00000354357.2:n.*184T>C
ENST00000429410.2:n.82+24539A>G (GSTM5)
NM_000849.4:c.*184T>C (GSTM3) NP_000840.2:n.*184T>C
NR_024537.1:n.1096T>C (GSTM3)
NM_000849.5:c.*184T>C (GSTM3) MANE Select NP_000840.2:n.*184T>C
NR_024537.2:n.1096T>C (GSTM3)