Canonical Allele Identifier: CA1092992494

Gene: FOXO3

Linked Data

• dbSNP Id: rs1776743617
• gnomAD v3: 6-108591967-A-G
• gnomAD v4: 6-108591967-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108591967A>G , CM000668.2:g.108591967A>G	GRCh38
NC_000006.11:g.108913170A>G , CM000668.1:g.108913170A>G	GRCh37
NC_000006.10:g.109019863A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406360.2:c.621+30138A>G MANE Select	ENSP00000385824.1:n.621+30138A>G
ENST00000343882.10:c.621+30138A>G	ENSP00000339527.6:n.621+30138A>G
ENST00000406360.1:c.621+30138A>G	ENSP00000385824.1:n.621+30138A>G
NM_001455.3:c.621+30138A>G	NP_001446.1:n.621+30138A>G
NM_201559.2:c.621+30138A>G	NP_963853.1:n.621+30138A>G
XM_005266867.3:c.-64+30138A>G	XP_005266924.1:n.-64+30138A>G
XM_011535626.1:c.120+29824A>G	XP_011533928.1:n.120+29824A>G
XM_011535627.1:c.69+5331A>G	XP_011533929.1:n.69+5331A>G
XM_011535628.1:c.-40+2152A>G	XP_011533930.1:n.-40+2152A>G
XM_005266867.4:c.-64+30138A>G	XP_005266924.1:n.-64+30138A>G
XM_011535626.2:c.120+29824A>G	XP_011533928.1:n.120+29824A>G
XM_011535628.3:c.-40+2152A>G	XP_011533930.1:n.-40+2152A>G
XM_017010585.1:c.-64+22225A>G	XP_016866074.1:n.-64+22225A>G
XM_017010586.1:c.-40+22225A>G	XP_016866075.1:n.-40+22225A>G
NM_001455.4:c.621+30138A>G MANE Select	NP_001446.1:n.621+30138A>G
NM_201559.3:c.621+30138A>G	NP_963853.1:n.621+30138A>G