Canonical Allele Identifier: CA2086517952
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1877454582
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644558A>T , CM000675.2:g.40644558A>T GRCh38
NC_000013.10:g.41218695A>T , CM000675.1:g.41218695A>T GRCh37
NC_000013.9:g.40116695A>T NCBI36
NG_023244.1:g.27040T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21025T>A MANE Select ENSP00000368880.4:n.630+21025T>A
ENST00000655267.1:n.333+21025T>A
ENST00000660760.1:n.296-11310T>A
ENST00000379561.5:c.630+21025T>A ENSP00000368880.4:n.630+21025T>A
NM_002015.3:c.630+21025T>A NP_002006.2:n.630+21025T>A
XR_941536.1:n.1226+781T>A
NM_002015.4:c.630+21025T>A MANE Select NP_002006.2:n.630+21025T>A
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