Canonical Allele Identifier: CA12245900
Gene: FOXO3 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.108656460T>C
GRCh37 chr6:g.108977663T>C
gnomAD v2:
6:108977663 T / C
gnomAD v3:
6:108656460 T / C
gnomAD v4:
chr6-108656460-T-C
Joint Max Group AF 0.70237325 (NFE)
Genomes Max Group AF 0.68757013 (NFE)
Exomes Max Group AF 0.70329484 (NFE)
dbSNP:
9400239
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108656460T>C , CM000668.2:g.108656460T>C GRCh38
NC_000006.11:g.108977663T>C , CM000668.1:g.108977663T>C GRCh37
NC_000006.10:g.109084356T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.622-6995T>C MANE Select ENSP00000385824.1:n.622-6995T>C
ENST00000343882.10:c.622-6995T>C ENSP00000339527.6:n.622-6995T>C
ENST00000406360.1:c.622-6995T>C ENSP00000385824.1:n.622-6995T>C
ENST00000540898.1:c.-118T>C ENSP00000446316.1:n.-118T>C
NM_001455.3:c.622-6995T>C NP_001446.1:n.622-6995T>C
NM_201559.2:c.622-6995T>C NP_963853.1:n.622-6995T>C
XM_005266867.3:c.55-6995T>C XP_005266924.1:n.55-6995T>C
XM_005266868.2:c.-118T>C XP_005266925.1:n.-118T>C
XM_011535626.1:c.121-6995T>C XP_011533928.1:n.121-6995T>C
XM_011535627.1:c.70-6995T>C XP_011533929.1:n.70-6995T>C
XM_011535628.1:c.-39-6995T>C XP_011533930.1:n.-39-6995T>C
XM_011535629.1:c.-40+95T>C XP_011533931.1:n.-40+95T>C
XM_005266867.4:c.55-6995T>C XP_005266924.1:n.55-6995T>C
XM_005266868.3:c.-118T>C XP_005266925.1:n.-118T>C
XM_011535626.2:c.121-6995T>C XP_011533928.1:n.121-6995T>C
XM_011535628.3:c.-39-6995T>C XP_011533930.1:n.-39-6995T>C
XM_011535629.2:c.-40+95T>C XP_011533931.1:n.-40+95T>C
XM_017010585.1:c.55-6995T>C XP_016866074.1:n.55-6995T>C
XM_017010586.1:c.-39-6995T>C XP_016866075.1:n.-39-6995T>C
NM_001455.4:c.622-6995T>C MANE Select NP_001446.1:n.622-6995T>C
NM_201559.3:c.622-6995T>C NP_963853.1:n.622-6995T>C
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