Canonical Allele Identifier: CA212451559
Gene: GSTO1 HGNC NCBI

Linked Data

dbSNP Id: rs1804834
gnomAD v4: 10-104263044-A-G
MyVariant Identifiers: chr10:g.106022802A>G (hg19) chr10:g.104263044A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104263044A>G , CM000672.2:g.104263044A>G GRCh38
NC_000010.10:g.106022802A>G , CM000672.1:g.106022802A>G GRCh37
NC_000010.9:g.106012792A>G NCBI36
NG_023362.1:g.13851A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369713.10:c.432A>G MANE Select ENSP00000358727.5:p.Glu144=
ENST00000369710.8:c.367-3040A>G ENSP00000358724.4:n.367-3040A>G
ENST00000369713.9:c.432A>G ENSP00000358727.5:p.Glu144=
ENST00000432659.1:c.283-3040A>G ENSP00000405325.1:n.283-3040A>G
ENST00000445155.5:c.348A>G ENSP00000406708.1:p.Glu116=
ENST00000493946.1:n.734A>G
ENST00000539281.5:c.348A>G ENSP00000441488.1:p.Glu116=
NM_001191002.1:c.367-3040A>G NP_001177931.1:n.367-3040A>G
NM_001191003.1:c.348A>G NP_001177932.1:p.Glu116=
NM_004832.2:c.432A>G NP_004823.1:p.Glu144=
NM_004832.3:c.432A>G MANE Select NP_004823.1:p.Glu144=
NM_001191002.2:c.367-3040A>G NP_001177931.1:n.367-3040A>G
NM_001191003.2:c.348A>G NP_001177932.1:p.Glu116=
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