Canonical Allele Identifier: CA12994268
Gene: FOXE1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.97853632A>G
GRCh37 chr9:g.100615914A>G
gnomAD v2:
9:100615914 A / G
gnomAD v3:
9:97853632 A / G
gnomAD v4:
chr9-97853632-A-G
Joint Max Group AF 0.86489262 (EAS)
Genomes Max Group AF 0.86527482 (EAS)
Exomes Max Group AF 0.85998307 (EAS)
ClinVar RCV:
RCV001725006
ClinVar Variation:
1297302
dbSNP:
1867277
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853632A>G , CM000671.2:g.97853632A>G GRCh38
NC_000009.11:g.100615914A>G , CM000671.1:g.100615914A>G GRCh37
NC_000009.10:g.99655735A>G NCBI36
NG_011979.1:g.5378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375123.5:c.-283A>G MANE Select ENSP00000364265.3:n.-283A>G
ENST00000375123.4:c.-283A>G ENSP00000364265.3:n.-283A>G
NM_004473.3:c.-283A>G NP_004464.2:n.-283A>G
NM_004473.4:c.-283A>G MANE Select NP_004464.2:n.-283A>G
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