Canonical Allele Identifier: CA16043517
Gene: FOXF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374061
dbSNP Id: rs1057518868

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510849A>T , CM000678.2:g.86510849A>T GRCh38
NC_000016.9:g.86544455A>T , CM000678.1:g.86544455A>T GRCh37
NC_000016.8:g.85101956A>T NCBI36
NG_016273.1:g.5323A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.280A>T MANE Select ENSP00000262426.4:p.Asn94Tyr
ENST00000262426.5:c.280A>T ENSP00000262426.4:p.Asn94Tyr
NM_001451.2:c.280A>T NP_001442.2:p.Asn94Tyr
NM_001451.3:c.280A>T MANE Select NP_001442.2:p.Asn94Tyr