Canonical Allele Identifier: CA419374480

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs1181167417
• gnomAD v2: 1-110279744-C-T
• gnomAD v4: 1-109737122-C-T
• MyVariant Identifiers: chr1:g.110279744C>T (hg19) ; chr1:g.109737122C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737122C>T , CM000663.2:g.109737122C>T	GRCh38
NC_000001.10:g.110279744C>T , CM000663.1:g.110279744C>T	GRCh37
NC_000001.9:g.110081267C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.627G>A (GSTM3) MANE Select	ENSP00000354357.2:p.Lys209=
ENST00000256594.7:c.627G>A (GSTM3)	ENSP00000256594.3:p.Lys209=
ENST00000361066.6:c.627G>A (GSTM3)	ENSP00000354357.2:p.Lys209=
ENST00000429410.2:n.82+24774C>T (GSTM5)
ENST00000476321.5:n.595G>A (GSTM3)
ENST00000486823.5:n.591G>A (GSTM3)
ENST00000488824.1:n.972G>A (GSTM3)
NM_000849.4:c.627G>A (GSTM3)	NP_000840.2:p.Lys209=
NR_024537.1:n.861G>A (GSTM3)
XM_011541296.1:c.846G>A (GSTM3)	XP_011539598.1:p.Lys282=
NM_000849.5:c.627G>A (GSTM3) MANE Select	NP_000840.2:p.Lys209=
NR_024537.2:n.861G>A (GSTM3)