Canonical Allele Identifier: CA419374512
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

gnomAD v4: 1-109737152-A-G
MyVariant Identifiers: chr1:g.110279774A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737152A>G , CM000663.2:g.109737152A>G GRCh38
NC_000001.10:g.110279774A>G , CM000663.1:g.110279774A>G GRCh37
NC_000001.9:g.110081297A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.597T>C (GSTM3) MANE Select ENSP00000354357.2:p.Ala199=
ENST00000256594.7:c.597T>C (GSTM3) ENSP00000256594.3:p.Ala199=
ENST00000361066.6:c.597T>C (GSTM3) ENSP00000354357.2:p.Ala199=
ENST00000429410.2:n.82+24804A>G (GSTM5)
ENST00000476321.5:n.565T>C (GSTM3)
ENST00000486823.5:n.561T>C (GSTM3)
ENST00000488824.1:n.942T>C (GSTM3)
NM_000849.4:c.597T>C (GSTM3) NP_000840.2:p.Ala199=
NR_024537.1:n.831T>C (GSTM3)
XM_011541296.1:c.816T>C (GSTM3) XP_011539598.1:p.Ala272=
NM_000849.5:c.597T>C (GSTM3) MANE Select NP_000840.2:p.Ala199=
NR_024537.2:n.831T>C (GSTM3)
Search 100 bp 5'
Search 100 bp 3'