Canonical Allele Identifier: CA397005821
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.280A>C MANE Select ENSP00000262426.4:p.Asn94His
ENST00000262426.5:c.280A>C ENSP00000262426.4:p.Asn94His
NM_001451.2:c.280A>C NP_001442.2:p.Asn94His
NM_001451.3:c.280A>C MANE Select NP_001442.2:p.Asn94His