Canonical Allele Identifier: CA2603197301

Linked Data

dbSNP Id: rs2101348514

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736762C>A , CM000663.2:g.109736762C>A GRCh38
NC_000001.10:g.110279384C>A , CM000663.1:g.110279384C>A GRCh37
NC_000001.9:g.110080907C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*309G>T (GSTM3) MANE Select ENSP00000354357.2:n.*309G>T
ENST00000256594.7:c.*309G>T (GSTM3) ENSP00000256594.3:n.*309G>T
ENST00000361066.6:c.*309G>T (GSTM3) ENSP00000354357.2:n.*309G>T
ENST00000429410.2:n.82+24414C>A (GSTM5)
NM_000849.4:c.*309G>T (GSTM3) NP_000840.2:n.*309G>T
NR_024537.1:n.1221G>T (GSTM3)
NM_000849.5:c.*309G>T (GSTM3) MANE Select NP_000840.2:n.*309G>T
NR_024537.2:n.1221G>T (GSTM3)