Canonical Allele Identifier: CA698022609
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1427881742
MyVariant Identifiers: chr13:g.41218737G>T (hg19) chr13:g.40644600G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644600G>T , CM000675.2:g.40644600G>T GRCh38
NC_000013.10:g.41218737G>T , CM000675.1:g.41218737G>T GRCh37
NC_000013.9:g.40116737G>T NCBI36
NG_023244.1:g.26998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+20983C>A MANE Select ENSP00000368880.4:n.630+20983C>A
ENST00000655267.1:n.333+20983C>A
ENST00000660760.1:n.296-11352C>A
ENST00000379561.5:c.630+20983C>A ENSP00000368880.4:n.630+20983C>A
NM_002015.3:c.630+20983C>A NP_002006.2:n.630+20983C>A
XR_941536.1:n.1226+739C>A
NM_002015.4:c.630+20983C>A MANE Select NP_002006.2:n.630+20983C>A
Search 100 bp 5'
Search 100 bp 3'