Canonical Allele Identifier: CA994837

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs777641323
• ExAC: 1:110279792 C / G
• gnomAD v2: 1-110279792-C-G
• gnomAD v3: 1-109737170-C-G
• gnomAD v4: 1-109737170-C-G
• MyVariant Identifiers: chr1:g.110279792C>G (hg19) ; chr1:g.109737170C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737170C>G , CM000663.2:g.109737170C>G	GRCh38
NC_000001.10:g.110279792C>G , CM000663.1:g.110279792C>G	GRCh37
NC_000001.9:g.110081315C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.580-1G>C (GSTM3) MANE Select	ENSP00000354357.2:n.580-1G>C
ENST00000256594.7:c.580-1G>C (GSTM3)	ENSP00000256594.3:n.580-1G>C
ENST00000361066.6:c.580-1G>C (GSTM3)	ENSP00000354357.2:n.580-1G>C
ENST00000429410.2:n.82+24822C>G (GSTM5)
ENST00000476321.5:n.547G>C (GSTM3)
ENST00000486823.5:n.544-1G>C (GSTM3)
ENST00000488824.1:n.925-1G>C (GSTM3)
NM_000849.4:c.580-1G>C (GSTM3)	NP_000840.2:n.580-1G>C
NR_024537.1:n.814-1G>C (GSTM3)
XM_011541296.1:c.799-1G>C (GSTM3)	XP_011539598.1:n.799-1G>C
NM_000849.5:c.580-1G>C (GSTM3) MANE Select	NP_000840.2:n.580-1G>C
NR_024537.2:n.814-1G>C (GSTM3)