Canonical Allele Identifier: CA365338802
Gene: FOXO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.108882976C>A (hg19) chr6:g.108561773C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561773C>A , CM000668.2:g.108561773C>A GRCh38
NC_000006.11:g.108882976C>A , CM000668.1:g.108882976C>A GRCh37
NC_000006.10:g.108989669C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.565C>A MANE Select ENSP00000385824.1:p.Arg189Ser
ENST00000343882.10:c.565C>A ENSP00000339527.6:p.Arg189Ser
ENST00000406360.1:c.565C>A ENSP00000385824.1:p.Arg189Ser
NM_001455.3:c.565C>A NP_001446.1:p.Arg189Ser
NM_201559.2:c.565C>A NP_963853.1:p.Arg189Ser
XM_005266867.3:c.-120C>A XP_005266924.1:n.-120C>A
XM_005266867.4:c.-120C>A XP_005266924.1:n.-120C>A
NM_001455.4:c.565C>A MANE Select NP_001446.1:p.Arg189Ser
NM_201559.3:c.565C>A NP_963853.1:p.Arg189Ser
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