Canonical Allele Identifier: CA341535817

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs766893669
• gnomAD v2: 1-110279769-T-G
• gnomAD v4: 1-109737147-T-G
• MyVariant Identifiers: chr1:g.110279769T>G (hg19) ; chr1:g.109737147T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737147T>G , CM000663.2:g.109737147T>G	GRCh38
NC_000001.10:g.110279769T>G , CM000663.1:g.110279769T>G	GRCh37
NC_000001.9:g.110081292T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.602A>C (GSTM3) MANE Select	ENSP00000354357.2:p.Tyr201Ser
ENST00000256594.7:c.602A>C (GSTM3)	ENSP00000256594.3:p.Tyr201Ser
ENST00000361066.6:c.602A>C (GSTM3)	ENSP00000354357.2:p.Tyr201Ser
ENST00000429410.2:n.82+24799T>G (GSTM5)
ENST00000476321.5:n.570A>C (GSTM3)
ENST00000486823.5:n.566A>C (GSTM3)
ENST00000488824.1:n.947A>C (GSTM3)
NM_000849.4:c.602A>C (GSTM3)	NP_000840.2:p.Tyr201Ser
NR_024537.1:n.836A>C (GSTM3)
XM_011541296.1:c.821A>C (GSTM3)	XP_011539598.1:p.Tyr274Ser
NM_000849.5:c.602A>C (GSTM3) MANE Select	NP_000840.2:p.Tyr201Ser
NR_024537.2:n.836A>C (GSTM3)