Canonical Allele Identifier: CA397005608
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510800C>A , CM000678.2:g.86510800C>A GRCh38
NC_000016.9:g.86544406C>A , CM000678.1:g.86544406C>A GRCh37
NC_000016.8:g.85101907C>A NCBI36
NG_016273.1:g.5274C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.231C>A MANE Select ENSP00000262426.4:p.Phe77Leu
ENST00000262426.5:c.231C>A ENSP00000262426.4:p.Phe77Leu
NM_001451.2:c.231C>A NP_001442.2:p.Phe77Leu
NM_001451.3:c.231C>A MANE Select NP_001442.2:p.Phe77Leu