Canonical Allele Identifier: CA341535469

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737081-G-T
• MyVariant Identifiers: chr1:g.110279703G>T (hg19) ; chr1:g.109737081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737081G>T , CM000663.2:g.109737081G>T	GRCh38
NC_000001.10:g.110279703G>T , CM000663.1:g.110279703G>T	GRCh37
NC_000001.9:g.110081226G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361066.7:c.668C>A (GSTM3) MANE Select	ENSP00000354357.2:p.Pro223His
ENST00000256594.7:c.668C>A (GSTM3)	ENSP00000256594.3:p.Pro223His
ENST00000361066.6:c.668C>A (GSTM3)	ENSP00000354357.2:p.Pro223His
ENST00000429410.2:n.82+24733G>T (GSTM5)
ENST00000476321.5:n.636C>A (GSTM3)
ENST00000486823.5:n.632C>A (GSTM3)
ENST00000488824.1:n.1013C>A (GSTM3)
NM_000849.4:c.668C>A (GSTM3)	NP_000840.2:p.Pro223His
NR_024537.1:n.902C>A (GSTM3)
XM_011541296.1:c.887C>A (GSTM3)	XP_011539598.1:p.Pro296His
NM_000849.5:c.668C>A (GSTM3) MANE Select	NP_000840.2:p.Pro223His
NR_024537.2:n.902C>A (GSTM3)