Canonical Allele Identifier: CA419374281

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs1265410633
• gnomAD v2: 1-110279637-G-C
• gnomAD v3: 1-109737015-G-C
• gnomAD v4: 1-109737015-G-C
• MyVariant Identifiers: chr1:g.110279637G>C (hg19) ; chr1:g.109737015G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737015G>C , CM000663.2:g.109737015G>C	GRCh38
NC_000001.10:g.110279637G>C , CM000663.1:g.110279637G>C	GRCh37
NC_000001.9:g.110081160G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.*56C>G (GSTM3) MANE Select	ENSP00000354357.2:n.*56C>G
ENST00000256594.7:c.*56C>G (GSTM3)	ENSP00000256594.3:n.*56C>G
ENST00000361066.6:c.*56C>G (GSTM3)	ENSP00000354357.2:n.*56C>G
ENST00000429410.2:n.82+24667G>C (GSTM5)
ENST00000476321.5:n.702C>G (GSTM3)
ENST00000486823.5:n.698C>G (GSTM3)
ENST00000488824.1:n.1079C>G (GSTM3)
NM_000849.4:c.*56C>G (GSTM3)	NP_000840.2:n.*56C>G
NR_024537.1:n.968C>G (GSTM3)
XM_011541296.1:c.*56C>G (GSTM3)	XP_011539598.1:n.*56C>G
NM_000849.5:c.*56C>G (GSTM3) MANE Select	NP_000840.2:n.*56C>G
NR_024537.2:n.968C>G (GSTM3)