Canonical Allele Identifier: CA698022327
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1170137037
gnomAD v3: 13-40644085-C-A
gnomAD v4: 13-40644085-C-A
MyVariant Identifiers: chr13:g.41218222C>A (hg19) chr13:g.40644085C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644085C>A , CM000675.2:g.40644085C>A GRCh38
NC_000013.10:g.41218222C>A , CM000675.1:g.41218222C>A GRCh37
NC_000013.9:g.40116222C>A NCBI36
NG_023244.1:g.27513G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21498G>T MANE Select ENSP00000368880.4:n.630+21498G>T
ENST00000655267.1:n.333+21498G>T
ENST00000660760.1:n.296-10837G>T
ENST00000379561.5:c.630+21498G>T ENSP00000368880.4:n.630+21498G>T
NM_002015.3:c.630+21498G>T NP_002006.2:n.630+21498G>T
XR_941536.1:n.1226+1254G>T
NM_002015.4:c.630+21498G>T MANE Select NP_002006.2:n.630+21498G>T
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