Canonical Allele Identifier: CA2578707561
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561846G>C , CM000668.2:g.108561846G>C GRCh38
NC_000006.11:g.108883049G>C , CM000668.1:g.108883049G>C GRCh37
NC_000006.10:g.108989742G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.621+17G>C MANE Select ENSP00000385824.1:n.621+17G>C
ENST00000343882.10:c.621+17G>C ENSP00000339527.6:n.621+17G>C
ENST00000406360.1:c.621+17G>C ENSP00000385824.1:n.621+17G>C
NM_001455.3:c.621+17G>C NP_001446.1:n.621+17G>C
NM_201559.2:c.621+17G>C NP_963853.1:n.621+17G>C
XM_005266867.3:c.-64+17G>C XP_005266924.1:n.-64+17G>C
XM_005266867.4:c.-64+17G>C XP_005266924.1:n.-64+17G>C
NM_001455.4:c.621+17G>C MANE Select NP_001446.1:n.621+17G>C
NM_201559.3:c.621+17G>C NP_963853.1:n.621+17G>C