Canonical Allele Identifier: CA145712191
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs949166793
gnomAD v4: 6-108561552-C-T
MyVariant Identifiers: chr6:g.108882755C>T (hg19) chr6:g.108561552C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561552C>T , CM000668.2:g.108561552C>T GRCh38
NC_000006.11:g.108882755C>T , CM000668.1:g.108882755C>T GRCh37
NC_000006.10:g.108989448C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.344C>T MANE Select ENSP00000385824.1:p.Ala115Val
ENST00000343882.10:c.344C>T ENSP00000339527.6:p.Ala115Val
ENST00000406360.1:c.344C>T ENSP00000385824.1:p.Ala115Val
NM_001455.3:c.344C>T NP_001446.1:p.Ala115Val
NM_201559.2:c.344C>T NP_963853.1:p.Ala115Val
NM_001455.4:c.344C>T MANE Select NP_001446.1:p.Ala115Val
NM_201559.3:c.344C>T NP_963853.1:p.Ala115Val
Search 100 bp 5'
Search 100 bp 3'