Canonical Allele Identifier: CA2239913453
Gene: FOXF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510805A= , CM000678.2:g.86510805A= GRCh38
NC_000016.9:g.86544411A= , CM000678.1:g.86544411A= GRCh37
NC_000016.8:g.85101912A= NCBI36
NG_016273.1:g.5279A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.236A= MANE Select ENSP00000262426.4:p.Gln79=
ENST00000262426.5:c.236A= ENSP00000262426.4:p.Gln79=
NM_001451.2:c.236A= NP_001442.2:p.Gln79=
NM_001451.3:c.236A= MANE Select NP_001442.2:p.Gln79=