Canonical Allele Identifier: CA419374441

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737080-A-C
• MyVariant Identifiers: chr1:g.110279702A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737080A>C , CM000663.2:g.109737080A>C	GRCh38
NC_000001.10:g.110279702A>C , CM000663.1:g.110279702A>C	GRCh37
NC_000001.9:g.110081225A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361066.7:c.669T>G (GSTM3) MANE Select	ENSP00000354357.2:p.Pro223=
ENST00000256594.7:c.669T>G (GSTM3)	ENSP00000256594.3:p.Pro223=
ENST00000361066.6:c.669T>G (GSTM3)	ENSP00000354357.2:p.Pro223=
ENST00000429410.2:n.82+24732A>C (GSTM5)
ENST00000476321.5:n.637T>G (GSTM3)
ENST00000486823.5:n.633T>G (GSTM3)
ENST00000488824.1:n.1014T>G (GSTM3)
NM_000849.4:c.669T>G (GSTM3)	NP_000840.2:p.Pro223=
NR_024537.1:n.903T>G (GSTM3)
XM_011541296.1:c.888T>G (GSTM3)	XP_011539598.1:p.Pro296=
NM_000849.5:c.669T>G (GSTM3) MANE Select	NP_000840.2:p.Pro223=
NR_024537.2:n.903T>G (GSTM3)