Canonical Allele Identifier: CA397005842
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510853C>T , CM000678.2:g.86510853C>T GRCh38
NC_000016.9:g.86544459C>T , CM000678.1:g.86544459C>T GRCh37
NC_000016.8:g.85101960C>T NCBI36
NG_016273.1:g.5327C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.284C>T MANE Select ENSP00000262426.4:p.Ser95Phe
ENST00000262426.5:c.284C>T ENSP00000262426.4:p.Ser95Phe
NM_001451.2:c.284C>T NP_001442.2:p.Ser95Phe
NM_001451.3:c.284C>T MANE Select NP_001442.2:p.Ser95Phe