Canonical Allele Identifier: CA28692758
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2515079
ClinVar RCV Id: RCV004293681
dbSNP Id: rs969716985
gnomAD v2: 1-110279791-C-G
gnomAD v3: 1-109737169-C-G
gnomAD v4: 1-109737169-C-G
MyVariant Identifiers: chr1:g.110279791C>G (hg19) chr1:g.109737169C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737169C>G , CM000663.2:g.109737169C>G GRCh38
NC_000001.10:g.110279791C>G , CM000663.1:g.110279791C>G GRCh37
NC_000001.9:g.110081314C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580G>C (GSTM3) MANE Select ENSP00000354357.2:p.Ala194Pro
ENST00000256594.7:c.580G>C (GSTM3) ENSP00000256594.3:p.Ala194Pro
ENST00000361066.6:c.580G>C (GSTM3) ENSP00000354357.2:p.Ala194Pro
ENST00000429410.2:n.82+24821C>G (GSTM5)
ENST00000476321.5:n.548G>C (GSTM3)
ENST00000486823.5:n.544G>C (GSTM3)
ENST00000488824.1:n.925G>C (GSTM3)
NM_000849.4:c.580G>C (GSTM3) NP_000840.2:p.Ala194Pro
NR_024537.1:n.814G>C (GSTM3)
XM_011541296.1:c.799G>C (GSTM3) XP_011539598.1:p.Ala267Pro
NM_000849.5:c.580G>C (GSTM3) MANE Select NP_000840.2:p.Ala194Pro
NR_024537.2:n.814G>C (GSTM3)
Search 100 bp 5'
Search 100 bp 3'