Canonical Allele Identifier: CA28692631

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs2234696
• MyVariant Identifiers: chr1:g.110279602T>C (hg19) ; chr1:g.109736980T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109736980T>C , CM000663.2:g.109736980T>C	GRCh38
NC_000001.10:g.110279602T>C , CM000663.1:g.110279602T>C	GRCh37
NC_000001.9:g.110081125T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.*91A>G (GSTM3) MANE Select	ENSP00000354357.2:n.*91A>G
ENST00000256594.7:c.*91A>G (GSTM3)	ENSP00000256594.3:n.*91A>G
ENST00000361066.6:c.*91A>G (GSTM3)	ENSP00000354357.2:n.*91A>G
ENST00000429410.2:n.82+24632T>C (GSTM5)
ENST00000476321.5:n.737A>G (GSTM3)
ENST00000486823.5:n.733A>G (GSTM3)
ENST00000488824.1:n.1114A>G (GSTM3)
NM_000849.4:c.*91A>G (GSTM3)	NP_000840.2:n.*91A>G
NR_024537.1:n.1003A>G (GSTM3)
XM_011541296.1:c.*91A>G (GSTM3)	XP_011539598.1:n.*91A>G
NM_000849.5:c.*91A>G (GSTM3) MANE Select	NP_000840.2:n.*91A>G
NR_024537.2:n.1003A>G (GSTM3)