Canonical Allele Identifier: CA419374391
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

gnomAD v4: 1-109737054-G-T
MyVariant Identifiers: chr1:g.110279676G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737054G>T , CM000663.2:g.109737054G>T GRCh38
NC_000001.10:g.110279676G>T , CM000663.1:g.110279676G>T GRCh37
NC_000001.9:g.110081199G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*17C>A (GSTM3) MANE Select ENSP00000354357.2:n.*17C>A
ENST00000256594.7:c.*17C>A (GSTM3) ENSP00000256594.3:n.*17C>A
ENST00000361066.6:c.*17C>A (GSTM3) ENSP00000354357.2:n.*17C>A
ENST00000429410.2:n.82+24706G>T (GSTM5)
ENST00000476321.5:n.663C>A (GSTM3)
ENST00000486823.5:n.659C>A (GSTM3)
ENST00000488824.1:n.1040C>A (GSTM3)
NM_000849.4:c.*17C>A (GSTM3) NP_000840.2:n.*17C>A
NR_024537.1:n.929C>A (GSTM3)
XM_011541296.1:c.*17C>A (GSTM3) XP_011539598.1:n.*17C>A
NM_000849.5:c.*17C>A (GSTM3) MANE Select NP_000840.2:n.*17C>A
NR_024537.2:n.929C>A (GSTM3)
Search 100 bp 5'
Search 100 bp 3'