Canonical Allele Identifier: CA2646987214

Linked Data

Genomic Alleles

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

Transcript Alleles

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