Canonical Allele Identifier: CA994833

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs199933862
• ExAC: 1:110279776 C / T
• gnomAD v2: 1-110279776-C-T
• gnomAD v3: 1-109737154-C-T
• gnomAD v4: 1-109737154-C-T
• MyVariant Identifiers: chr1:g.110279776C>T (hg19) ; chr1:g.109737154C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737154C>T , CM000663.2:g.109737154C>T	GRCh38
NC_000001.10:g.110279776C>T , CM000663.1:g.110279776C>T	GRCh37
NC_000001.9:g.110081299C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.595G>A (GSTM3) MANE Select	ENSP00000354357.2:p.Ala199Thr
ENST00000256594.7:c.595G>A (GSTM3)	ENSP00000256594.3:p.Ala199Thr
ENST00000361066.6:c.595G>A (GSTM3)	ENSP00000354357.2:p.Ala199Thr
ENST00000429410.2:n.82+24806C>T (GSTM5)
ENST00000476321.5:n.563G>A (GSTM3)
ENST00000486823.5:n.559G>A (GSTM3)
ENST00000488824.1:n.940G>A (GSTM3)
NM_000849.4:c.595G>A (GSTM3)	NP_000840.2:p.Ala199Thr
NR_024537.1:n.829G>A (GSTM3)
XM_011541296.1:c.814G>A (GSTM3)	XP_011539598.1:p.Ala272Thr
NM_000849.5:c.595G>A (GSTM3) MANE Select	NP_000840.2:p.Ala199Thr
NR_024537.2:n.829G>A (GSTM3)