Canonical Allele Identifier: CA2086517837
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1877445933
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644321C>T , CM000675.2:g.40644321C>T GRCh38
NC_000013.10:g.41218458C>T , CM000675.1:g.41218458C>T GRCh37
NC_000013.9:g.40116458C>T NCBI36
NG_023244.1:g.27277G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21262G>A MANE Select ENSP00000368880.4:n.630+21262G>A
ENST00000655267.1:n.333+21262G>A
ENST00000660760.1:n.296-11073G>A
ENST00000379561.5:c.630+21262G>A ENSP00000368880.4:n.630+21262G>A
NM_002015.3:c.630+21262G>A NP_002006.2:n.630+21262G>A
XR_941536.1:n.1226+1018G>A
NM_002015.4:c.630+21262G>A MANE Select NP_002006.2:n.630+21262G>A
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