Canonical Allele Identifier: CA419374182

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109736982-A-G
• MyVariant Identifiers: chr1:g.110279604A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109736982A>G , CM000663.2:g.109736982A>G	GRCh38
NC_000001.10:g.110279604A>G , CM000663.1:g.110279604A>G	GRCh37
NC_000001.9:g.110081127A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.*89T>C (GSTM3) MANE Select	ENSP00000354357.2:n.*89T>C
ENST00000256594.7:c.*89T>C (GSTM3)	ENSP00000256594.3:n.*89T>C
ENST00000361066.6:c.*89T>C (GSTM3)	ENSP00000354357.2:n.*89T>C
ENST00000429410.2:n.82+24634A>G (GSTM5)
ENST00000476321.5:n.735T>C (GSTM3)
ENST00000486823.5:n.731T>C (GSTM3)
ENST00000488824.1:n.1112T>C (GSTM3)
NM_000849.4:c.*89T>C (GSTM3)	NP_000840.2:n.*89T>C
NR_024537.1:n.1001T>C (GSTM3)
XM_011541296.1:c.*89T>C (GSTM3)	XP_011539598.1:n.*89T>C
NM_000849.5:c.*89T>C (GSTM3) MANE Select	NP_000840.2:n.*89T>C
NR_024537.2:n.1001T>C (GSTM3)