Canonical Allele Identifier: CA2239913448
Gene: FOXF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510797G= , CM000678.2:g.86510797G= GRCh38
NC_000016.9:g.86544403G= , CM000678.1:g.86544403G= GRCh37
NC_000016.8:g.85101904G= NCBI36
NG_016273.1:g.5271G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.228G= MANE Select ENSP00000262426.4:p.Gln76=
ENST00000262426.5:c.228G= ENSP00000262426.4:p.Gln76=
NM_001451.2:c.228G= NP_001442.2:p.Gln76=
NM_001451.3:c.228G= MANE Select NP_001442.2:p.Gln76=