Canonical Allele Identifier: CA885397201
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

dbSNP Id: rs1255854645
gnomAD v3: 1-109736707-C-T
gnomAD v4: 1-109736707-C-T
MyVariant Identifiers: chr1:g.110279329C>T (hg19) chr1:g.109736707C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736707C>T , CM000663.2:g.109736707C>T GRCh38
NC_000001.10:g.110279329C>T , CM000663.1:g.110279329C>T GRCh37
NC_000001.9:g.110080852C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*364G>A (GSTM3) MANE Select ENSP00000354357.2:n.*364G>A
ENST00000256594.7:c.*364G>A (GSTM3) ENSP00000256594.3:n.*364G>A
ENST00000361066.6:c.*364G>A (GSTM3) ENSP00000354357.2:n.*364G>A
ENST00000429410.2:n.82+24359C>T (GSTM5)
NM_000849.4:c.*364G>A (GSTM3) NP_000840.2:n.*364G>A
NR_024537.1:n.1276G>A (GSTM3)
NM_000849.5:c.*364G>A (GSTM3) MANE Select NP_000840.2:n.*364G>A
NR_024537.2:n.1276G>A (GSTM3)
Search 100 bp 5'
Search 100 bp 3'