Canonical Allele Identifier: CA569551557

Gene: FOXO3

Linked Data

• dbSNP Id: rs2490272
• gnomAD v2: 6-108895386-C-G
• gnomAD v3: 6-108574183-C-G
• gnomAD v4: 6-108574183-C-G
• MyVariant Identifiers: chr6:g.108895386C>G (hg19) ; chr6:g.108574183C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108574183C>G , CM000668.2:g.108574183C>G	GRCh38
NC_000006.11:g.108895386C>G , CM000668.1:g.108895386C>G	GRCh37
NC_000006.10:g.109002079C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.621+12354C>G MANE Select	ENSP00000385824.1:n.621+12354C>G
ENST00000343882.10:c.621+12354C>G	ENSP00000339527.6:n.621+12354C>G
ENST00000406360.1:c.621+12354C>G	ENSP00000385824.1:n.621+12354C>G
NM_001455.3:c.621+12354C>G	NP_001446.1:n.621+12354C>G
NM_201559.2:c.621+12354C>G	NP_963853.1:n.621+12354C>G
XM_005266867.3:c.-64+12354C>G	XP_005266924.1:n.-64+12354C>G
XM_011535626.1:c.120+12040C>G	XP_011533928.1:n.120+12040C>G
XM_005266867.4:c.-64+12354C>G	XP_005266924.1:n.-64+12354C>G
XM_011535626.2:c.120+12040C>G	XP_011533928.1:n.120+12040C>G
XM_017010585.1:c.-64+4441C>G	XP_016866074.1:n.-64+4441C>G
XM_017010586.1:c.-40+4441C>G	XP_016866075.1:n.-40+4441C>G
NM_001455.4:c.621+12354C>G MANE Select	NP_001446.1:n.621+12354C>G
NM_201559.3:c.621+12354C>G	NP_963853.1:n.621+12354C>G