Canonical Allele Identifier: CA525314185
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

dbSNP Id: rs1442415216
gnomAD v2: 1-110279398-C-G
gnomAD v3: 1-109736776-C-G
gnomAD v4: 1-109736776-C-G
MyVariant Identifiers: chr1:g.110279398C>G (hg19) chr1:g.109736776C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736776C>G , CM000663.2:g.109736776C>G GRCh38
NC_000001.10:g.110279398C>G , CM000663.1:g.110279398C>G GRCh37
NC_000001.9:g.110080921C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*295G>C (GSTM3) MANE Select ENSP00000354357.2:n.*295G>C
ENST00000256594.7:c.*295G>C (GSTM3) ENSP00000256594.3:n.*295G>C
ENST00000361066.6:c.*295G>C (GSTM3) ENSP00000354357.2:n.*295G>C
ENST00000429410.2:n.82+24428C>G (GSTM5)
NM_000849.4:c.*295G>C (GSTM3) NP_000840.2:n.*295G>C
NR_024537.1:n.1207G>C (GSTM3)
NM_000849.5:c.*295G>C (GSTM3) MANE Select NP_000840.2:n.*295G>C
NR_024537.2:n.1207G>C (GSTM3)
Search 100 bp 5'
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