Canonical Allele Identifier: CA609685240
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs981336488
gnomAD v2: 13-41218254-C-G
gnomAD v3: 13-40644117-C-G
gnomAD v4: 13-40644117-C-G
MyVariant Identifiers: chr13:g.41218254C>G (hg19) chr13:g.40644117C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644117C>G , CM000675.2:g.40644117C>G GRCh38
NC_000013.10:g.41218254C>G , CM000675.1:g.41218254C>G GRCh37
NC_000013.9:g.40116254C>G NCBI36
NG_023244.1:g.27481G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21466G>C MANE Select ENSP00000368880.4:n.630+21466G>C
ENST00000655267.1:n.333+21466G>C
ENST00000660760.1:n.296-10869G>C
ENST00000379561.5:c.630+21466G>C ENSP00000368880.4:n.630+21466G>C
NM_002015.3:c.630+21466G>C NP_002006.2:n.630+21466G>C
XR_941536.1:n.1226+1222G>C
NM_002015.4:c.630+21466G>C MANE Select NP_002006.2:n.630+21466G>C
Search 100 bp 5'
Search 100 bp 3'