Canonical Allele Identifier: CA419374352

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737041-C-T
• MyVariant Identifiers: chr1:g.110279663C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737041C>T , CM000663.2:g.109737041C>T	GRCh38
NC_000001.10:g.110279663C>T , CM000663.1:g.110279663C>T	GRCh37
NC_000001.9:g.110081186C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.*30G>A (GSTM3) MANE Select	ENSP00000354357.2:n.*30G>A
ENST00000256594.7:c.*30G>A (GSTM3)	ENSP00000256594.3:n.*30G>A
ENST00000361066.6:c.*30G>A (GSTM3)	ENSP00000354357.2:n.*30G>A
ENST00000429410.2:n.82+24693C>T (GSTM5)
ENST00000476321.5:n.676G>A (GSTM3)
ENST00000486823.5:n.672G>A (GSTM3)
ENST00000488824.1:n.1053G>A (GSTM3)
NM_000849.4:c.*30G>A (GSTM3)	NP_000840.2:n.*30G>A
NR_024537.1:n.942G>A (GSTM3)
XM_011541296.1:c.*30G>A (GSTM3)	XP_011539598.1:n.*30G>A
NM_000849.5:c.*30G>A (GSTM3) MANE Select	NP_000840.2:n.*30G>A
NR_024537.2:n.942G>A (GSTM3)