Canonical Allele Identifier: CA365338788
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561767A>C , CM000668.2:g.108561767A>C GRCh38
NC_000006.11:g.108882970A>C , CM000668.1:g.108882970A>C GRCh37
NC_000006.10:g.108989663A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.559A>C MANE Select ENSP00000385824.1:p.Met187Leu
ENST00000343882.10:c.559A>C ENSP00000339527.6:p.Met187Leu
ENST00000406360.1:c.559A>C ENSP00000385824.1:p.Met187Leu
NM_001455.3:c.559A>C NP_001446.1:p.Met187Leu
NM_201559.2:c.559A>C NP_963853.1:p.Met187Leu
XM_005266867.3:c.-126A>C XP_005266924.1:n.-126A>C
XM_005266867.4:c.-126A>C XP_005266924.1:n.-126A>C
NM_001455.4:c.559A>C MANE Select NP_001446.1:p.Met187Leu
NM_201559.3:c.559A>C NP_963853.1:p.Met187Leu