Canonical Allele Identifier: CA145724557

Gene: FOXO3

Linked Data

• dbSNP Id: rs570843235
• gnomAD v3: 6-108677752-A-C
• gnomAD v4: 6-108677752-A-C
• MyVariant Identifiers: chr6:g.108998955A>C (hg19) ; chr6:g.108677752A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108677752A>C , CM000668.2:g.108677752A>C	GRCh38
NC_000006.11:g.108998955A>C , CM000668.1:g.108998955A>C	GRCh37
NC_000006.10:g.109105648A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.*35-2075A>C MANE Select	ENSP00000385824.1:n.*35-2075A>C
ENST00000343882.10:c.*35-2075A>C	ENSP00000339527.6:n.*35-2075A>C
ENST00000406360.1:c.*35-2075A>C	ENSP00000385824.1:n.*35-2075A>C
ENST00000540898.1:c.*35-2075A>C	ENSP00000446316.1:n.*35-2075A>C
NM_001455.3:c.*35-2075A>C	NP_001446.1:n.*35-2075A>C
NM_201559.2:c.*35-2075A>C	NP_963853.1:n.*35-2075A>C
XM_005266867.3:c.*35-2075A>C	XP_005266924.1:n.*35-2075A>C
XM_005266868.2:c.*35-2075A>C	XP_005266925.1:n.*35-2075A>C
XM_011535626.1:c.*35-2075A>C	XP_011533928.1:n.*35-2075A>C
XM_011535627.1:c.*35-2075A>C	XP_011533929.1:n.*35-2075A>C
XM_011535628.1:c.*35-2075A>C	XP_011533930.1:n.*35-2075A>C
XM_011535629.1:c.*35-2075A>C	XP_011533931.1:n.*35-2075A>C
XM_005266867.4:c.*35-2075A>C	XP_005266924.1:n.*35-2075A>C
XM_005266868.3:c.*35-2075A>C	XP_005266925.1:n.*35-2075A>C
XM_011535626.2:c.*35-2075A>C	XP_011533928.1:n.*35-2075A>C
XM_011535628.3:c.*35-2075A>C	XP_011533930.1:n.*35-2075A>C
XM_011535629.2:c.*35-2075A>C	XP_011533931.1:n.*35-2075A>C
XM_017010585.1:c.*35-2075A>C	XP_016866074.1:n.*35-2075A>C
XM_017010586.1:c.*35-2075A>C	XP_016866075.1:n.*35-2075A>C
NM_001455.4:c.*35-2075A>C MANE Select	NP_001446.1:n.*35-2075A>C
NM_201559.3:c.*35-2075A>C	NP_963853.1:n.*35-2075A>C