Canonical Allele Identifier: CA365338364
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs1225186329
gnomAD v2: 6-108882833-C-T
gnomAD v4: 6-108561630-C-T
MyVariant Identifiers: chr6:g.108882833C>T (hg19) chr6:g.108561630C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561630C>T , CM000668.2:g.108561630C>T GRCh38
NC_000006.11:g.108882833C>T , CM000668.1:g.108882833C>T GRCh37
NC_000006.10:g.108989526C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.422C>T MANE Select ENSP00000385824.1:p.Ala141Val
ENST00000343882.10:c.422C>T ENSP00000339527.6:p.Ala141Val
ENST00000406360.1:c.422C>T ENSP00000385824.1:p.Ala141Val
NM_001455.3:c.422C>T NP_001446.1:p.Ala141Val
NM_201559.2:c.422C>T NP_963853.1:p.Ala141Val
NM_001455.4:c.422C>T MANE Select NP_001446.1:p.Ala141Val
NM_201559.3:c.422C>T NP_963853.1:p.Ala141Val
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