Canonical Allele Identifier: CA1188220347

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736765A= , CM000663.2:g.109736765A= GRCh38
NC_000001.10:g.110279387A= , CM000663.1:g.110279387A= GRCh37
NC_000001.9:g.110080910A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*306T= (GSTM3) MANE Select ENSP00000354357.2:n.*306T=
ENST00000256594.7:c.*306T= (GSTM3) ENSP00000256594.3:n.*306T=
ENST00000361066.6:c.*306T= (GSTM3) ENSP00000354357.2:n.*306T=
ENST00000429410.2:n.82+24417A= (GSTM5)
NM_000849.4:c.*306T= (GSTM3) NP_000840.2:n.*306T=
NR_024537.1:n.1218T= (GSTM3)
NM_000849.5:c.*306T= (GSTM3) MANE Select NP_000840.2:n.*306T=
NR_024537.2:n.1218T= (GSTM3)