Canonical Allele Identifier: CA2086517902
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1877450398
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644451A>G , CM000675.2:g.40644451A>G GRCh38
NC_000013.10:g.41218588A>G , CM000675.1:g.41218588A>G GRCh37
NC_000013.9:g.40116588A>G NCBI36
NG_023244.1:g.27147T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21132T>C MANE Select ENSP00000368880.4:n.630+21132T>C
ENST00000655267.1:n.333+21132T>C
ENST00000660760.1:n.296-11203T>C
ENST00000379561.5:c.630+21132T>C ENSP00000368880.4:n.630+21132T>C
NM_002015.3:c.630+21132T>C NP_002006.2:n.630+21132T>C
XR_941536.1:n.1226+888T>C
NM_002015.4:c.630+21132T>C MANE Select NP_002006.2:n.630+21132T>C
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