Canonical Allele Identifier: CA365338942

Gene: FOXO3

Linked Data

• MyVariant Identifiers: chr6:g.108883034T>C (hg19) ; chr6:g.108561831T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108561831T>C , CM000668.2:g.108561831T>C	GRCh38
NC_000006.11:g.108883034T>C , CM000668.1:g.108883034T>C	GRCh37
NC_000006.10:g.108989727T>C	NCBI36

Transcript Alleles

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