Canonical Allele Identifier: CA698022499
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1313399164
MyVariant Identifiers: chr13:g.41218601T>G (hg19) chr13:g.40644464T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644464T>G , CM000675.2:g.40644464T>G GRCh38
NC_000013.10:g.41218601T>G , CM000675.1:g.41218601T>G GRCh37
NC_000013.9:g.40116601T>G NCBI36
NG_023244.1:g.27134A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21119A>C MANE Select ENSP00000368880.4:n.630+21119A>C
ENST00000655267.1:n.333+21119A>C
ENST00000660760.1:n.296-11216A>C
ENST00000379561.5:c.630+21119A>C ENSP00000368880.4:n.630+21119A>C
NM_002015.3:c.630+21119A>C NP_002006.2:n.630+21119A>C
XR_941536.1:n.1226+875A>C
NM_002015.4:c.630+21119A>C MANE Select NP_002006.2:n.630+21119A>C
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