Canonical Allele Identifier: CA2239913432
Gene: FOXF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510749C= , CM000678.2:g.86510749C= GRCh38
NC_000016.9:g.86544355C= , CM000678.1:g.86544355C= GRCh37
NC_000016.8:g.85101856C= NCBI36
NG_016273.1:g.5223C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.180C= MANE Select ENSP00000262426.4:p.Ala60=
ENST00000262426.5:c.180C= ENSP00000262426.4:p.Ala60=
NM_001451.2:c.180C= NP_001442.2:p.Ala60=
NM_001451.3:c.180C= MANE Select NP_001442.2:p.Ala60=