Canonical Allele Identifier: CA994811

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs780043117
• ExAC: 1:110279672 C / G
• gnomAD v2: 1-110279672-C-G
• gnomAD v3: 1-109737050-C-G
• gnomAD v4: 1-109737050-C-G
• MyVariant Identifiers: chr1:g.110279672C>G (hg19) ; chr1:g.109737050C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737050C>G , CM000663.2:g.109737050C>G	GRCh38
NC_000001.10:g.110279672C>G , CM000663.1:g.110279672C>G	GRCh37
NC_000001.9:g.110081195C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.*21G>C (GSTM3) MANE Select	ENSP00000354357.2:n.*21G>C
ENST00000256594.7:c.*21G>C (GSTM3)	ENSP00000256594.3:n.*21G>C
ENST00000361066.6:c.*21G>C (GSTM3)	ENSP00000354357.2:n.*21G>C
ENST00000429410.2:n.82+24702C>G (GSTM5)
ENST00000476321.5:n.667G>C (GSTM3)
ENST00000486823.5:n.663G>C (GSTM3)
ENST00000488824.1:n.1044G>C (GSTM3)
NM_000849.4:c.*21G>C (GSTM3)	NP_000840.2:n.*21G>C
NR_024537.1:n.933G>C (GSTM3)
XM_011541296.1:c.*21G>C (GSTM3)	XP_011539598.1:n.*21G>C
NM_000849.5:c.*21G>C (GSTM3) MANE Select	NP_000840.2:n.*21G>C
NR_024537.2:n.933G>C (GSTM3)