Canonical Allele Identifier: CA341535788

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737142-G-C
• MyVariant Identifiers: chr1:g.110279764G>C (hg19) ; chr1:g.109737142G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737142G>C , CM000663.2:g.109737142G>C	GRCh38
NC_000001.10:g.110279764G>C , CM000663.1:g.110279764G>C	GRCh37
NC_000001.9:g.110081287G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.607C>G (GSTM3) MANE Select	ENSP00000354357.2:p.Gln203Glu
ENST00000256594.7:c.607C>G (GSTM3)	ENSP00000256594.3:p.Gln203Glu
ENST00000361066.6:c.607C>G (GSTM3)	ENSP00000354357.2:p.Gln203Glu
ENST00000429410.2:n.82+24794G>C (GSTM5)
ENST00000476321.5:n.575C>G (GSTM3)
ENST00000486823.5:n.571C>G (GSTM3)
ENST00000488824.1:n.952C>G (GSTM3)
NM_000849.4:c.607C>G (GSTM3)	NP_000840.2:p.Gln203Glu
NR_024537.1:n.841C>G (GSTM3)
XM_011541296.1:c.826C>G (GSTM3)	XP_011539598.1:p.Gln276Glu
NM_000849.5:c.607C>G (GSTM3) MANE Select	NP_000840.2:p.Gln203Glu
NR_024537.2:n.841C>G (GSTM3)