Canonical Allele Identifier: CA419374017
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

dbSNP Id: rs1649215376
gnomAD v3: 1-109736956-A-T
gnomAD v4: 1-109736956-A-T
MyVariant Identifiers: chr1:g.110279578A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736956A>T , CM000663.2:g.109736956A>T GRCh38
NC_000001.10:g.110279578A>T , CM000663.1:g.110279578A>T GRCh37
NC_000001.9:g.110081101A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*115T>A (GSTM3) MANE Select ENSP00000354357.2:n.*115T>A
ENST00000256594.7:c.*115T>A (GSTM3) ENSP00000256594.3:n.*115T>A
ENST00000361066.6:c.*115T>A (GSTM3) ENSP00000354357.2:n.*115T>A
ENST00000429410.2:n.82+24608A>T (GSTM5)
ENST00000486823.5:n.757T>A (GSTM3)
NM_000849.4:c.*115T>A (GSTM3) NP_000840.2:n.*115T>A
NR_024537.1:n.1027T>A (GSTM3)
NM_000849.5:c.*115T>A (GSTM3) MANE Select NP_000840.2:n.*115T>A
NR_024537.2:n.1027T>A (GSTM3)
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