Canonical Allele Identifier: CA994853

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs55646044
• ExAC: 1:110279993 G / A
• gnomAD v2: 1-110279993-G-A
• gnomAD v3: 1-109737371-G-A
• gnomAD v4: 1-109737371-G-A
• MyVariant Identifiers: chr1:g.110279993G>A (hg19) ; chr1:g.109737371G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737371G>A , CM000663.2:g.109737371G>A	GRCh38
NC_000001.10:g.110279993G>A , CM000663.1:g.110279993G>A	GRCh37
NC_000001.9:g.110081516G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.579+86C>T (GSTM3) MANE Select	ENSP00000354357.2:n.579+86C>T
ENST00000256594.7:c.579+86C>T (GSTM3)	ENSP00000256594.3:n.579+86C>T
ENST00000361066.6:c.579+86C>T (GSTM3)	ENSP00000354357.2:n.579+86C>T
ENST00000429410.2:n.82+25023G>A (GSTM5)
ENST00000476321.5:n.346C>T (GSTM3)
ENST00000486823.5:n.543+86C>T (GSTM3)
ENST00000488824.1:n.924+86C>T (GSTM3)
ENST00000540225.2:c.*16C>T (GSTM3)	ENSP00000444978.2:n.*16C>T
NM_000849.4:c.579+86C>T (GSTM3)	NP_000840.2:n.579+86C>T
NR_024537.1:n.813+86C>T (GSTM3)
XM_011541296.1:c.798+86C>T (GSTM3)	XP_011539598.1:n.798+86C>T
NM_000849.5:c.579+86C>T (GSTM3) MANE Select	NP_000840.2:n.579+86C>T
NR_024537.2:n.813+86C>T (GSTM3)