Canonical Allele Identifier: CA365338165
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs1775788679
gnomAD v4: 6-108561597-A-G
MyVariant Identifiers: chr6:g.108882800A>G (hg19) chr6:g.108561597A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561597A>G , CM000668.2:g.108561597A>G GRCh38
NC_000006.11:g.108882800A>G , CM000668.1:g.108882800A>G GRCh37
NC_000006.10:g.108989493A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.389A>G MANE Select ENSP00000385824.1:p.Gln130Arg
ENST00000343882.10:c.389A>G ENSP00000339527.6:p.Gln130Arg
ENST00000406360.1:c.389A>G ENSP00000385824.1:p.Gln130Arg
NM_001455.3:c.389A>G NP_001446.1:p.Gln130Arg
NM_201559.2:c.389A>G NP_963853.1:p.Gln130Arg
NM_001455.4:c.389A>G MANE Select NP_001446.1:p.Gln130Arg
NM_201559.3:c.389A>G NP_963853.1:p.Gln130Arg
Search 100 bp 5'
Search 100 bp 3'