Canonical Allele Identifier: CA248982952
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs762599183
gnomAD v2: 13-41218693-A-G
gnomAD v3: 13-40644556-A-G
gnomAD v4: 13-40644556-A-G
MyVariant Identifiers: chr13:g.41218693A>G (hg19) chr13:g.40644556A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644556A>G , CM000675.2:g.40644556A>G GRCh38
NC_000013.10:g.41218693A>G , CM000675.1:g.41218693A>G GRCh37
NC_000013.9:g.40116693A>G NCBI36
NG_023244.1:g.27042T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.630+21027T>C MANE Select ENSP00000368880.4:n.630+21027T>C
ENST00000655267.1:n.333+21027T>C
ENST00000660760.1:n.296-11308T>C
ENST00000379561.5:c.630+21027T>C ENSP00000368880.4:n.630+21027T>C
NM_002015.3:c.630+21027T>C NP_002006.2:n.630+21027T>C
XR_941536.1:n.1226+783T>C
NM_002015.4:c.630+21027T>C MANE Select NP_002006.2:n.630+21027T>C
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