Canonical Allele Identifier: CA525627036

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs1383207905
• gnomAD v2: 1-110279989-A-G
• gnomAD v4: 1-109737367-A-G
• MyVariant Identifiers: chr1:g.110279989A>G (hg19) ; chr1:g.109737367A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737367A>G , CM000663.2:g.109737367A>G	GRCh38
NC_000001.10:g.110279989A>G , CM000663.1:g.110279989A>G	GRCh37
NC_000001.9:g.110081512A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.579+90T>C (GSTM3) MANE Select	ENSP00000354357.2:n.579+90T>C
ENST00000256594.7:c.579+90T>C (GSTM3)	ENSP00000256594.3:n.579+90T>C
ENST00000361066.6:c.579+90T>C (GSTM3)	ENSP00000354357.2:n.579+90T>C
ENST00000429410.2:n.82+25019A>G (GSTM5)
ENST00000476321.5:n.350T>C (GSTM3)
ENST00000486823.5:n.543+90T>C (GSTM3)
ENST00000488824.1:n.924+90T>C (GSTM3)
ENST00000540225.2:c.*20T>C (GSTM3)	ENSP00000444978.2:n.*20T>C
NM_000849.4:c.579+90T>C (GSTM3)	NP_000840.2:n.579+90T>C
NR_024537.1:n.813+90T>C (GSTM3)
XM_011541296.1:c.798+90T>C (GSTM3)	XP_011539598.1:n.798+90T>C
NM_000849.5:c.579+90T>C (GSTM3) MANE Select	NP_000840.2:n.579+90T>C
NR_024537.2:n.813+90T>C (GSTM3)