Canonical Allele Identifier: CA994814

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs201374956
• ExAC: 1:110279683 T / G
• gnomAD v2: 1-110279683-T-G
• gnomAD v3: 1-109737061-T-G
• gnomAD v4: 1-109737061-T-G
• MyVariant Identifiers: chr1:g.110279683T>G (hg19) ; chr1:g.109737061T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737061T>G , CM000663.2:g.109737061T>G	GRCh38
NC_000001.10:g.110279683T>G , CM000663.1:g.110279683T>G	GRCh37
NC_000001.9:g.110081206T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.*10A>C (GSTM3) MANE Select	ENSP00000354357.2:n.*10A>C
ENST00000256594.7:c.*10A>C (GSTM3)	ENSP00000256594.3:n.*10A>C
ENST00000361066.6:c.*10A>C (GSTM3)	ENSP00000354357.2:n.*10A>C
ENST00000429410.2:n.82+24713T>G (GSTM5)
ENST00000476321.5:n.656A>C (GSTM3)
ENST00000486823.5:n.652A>C (GSTM3)
ENST00000488824.1:n.1033A>C (GSTM3)
NM_000849.4:c.*10A>C (GSTM3)	NP_000840.2:n.*10A>C
NR_024537.1:n.922A>C (GSTM3)
XM_011541296.1:c.*10A>C (GSTM3)	XP_011539598.1:n.*10A>C
NM_000849.5:c.*10A>C (GSTM3) MANE Select	NP_000840.2:n.*10A>C
NR_024537.2:n.922A>C (GSTM3)