Canonical Allele Identifier: CA2519214503
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561853A>G , CM000668.2:g.108561853A>G GRCh38
NC_000006.11:g.108883056A>G , CM000668.1:g.108883056A>G GRCh37
NC_000006.10:g.108989749A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.621+24A>G MANE Select ENSP00000385824.1:n.621+24A>G
ENST00000343882.10:c.621+24A>G ENSP00000339527.6:n.621+24A>G
ENST00000406360.1:c.621+24A>G ENSP00000385824.1:n.621+24A>G
NM_001455.3:c.621+24A>G NP_001446.1:n.621+24A>G
NM_201559.2:c.621+24A>G NP_963853.1:n.621+24A>G
XM_005266867.3:c.-64+24A>G XP_005266924.1:n.-64+24A>G
XM_005266867.4:c.-64+24A>G XP_005266924.1:n.-64+24A>G
NM_001455.4:c.621+24A>G MANE Select NP_001446.1:n.621+24A>G
NM_201559.3:c.621+24A>G NP_963853.1:n.621+24A>G