Canonical Allele Identifier: CA2086517901
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1877450320

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644449T>C , CM000675.2:g.40644449T>C GRCh38
NC_000013.10:g.41218586T>C , CM000675.1:g.41218586T>C GRCh37
NC_000013.9:g.40116586T>C NCBI36
NG_023244.1:g.27149A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.630+21134A>G MANE Select ENSP00000368880.4:n.630+21134A>G
ENST00000655267.1:n.333+21134A>G
ENST00000660760.1:n.296-11201A>G
ENST00000379561.5:c.630+21134A>G ENSP00000368880.4:n.630+21134A>G
NM_002015.3:c.630+21134A>G NP_002006.2:n.630+21134A>G
XR_941536.1:n.1226+890A>G
NM_002015.4:c.630+21134A>G MANE Select NP_002006.2:n.630+21134A>G