Canonical Allele Identifier: CA2239913468
Gene: FOXF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510852T= , CM000678.2:g.86510852T= GRCh38
NC_000016.9:g.86544458T= , CM000678.1:g.86544458T= GRCh37
NC_000016.8:g.85101959T= NCBI36
NG_016273.1:g.5326T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.283T= MANE Select ENSP00000262426.4:p.Ser95=
ENST00000262426.5:c.283T= ENSP00000262426.4:p.Ser95=
NM_001451.2:c.283T= NP_001442.2:p.Ser95=
NM_001451.3:c.283T= MANE Select NP_001442.2:p.Ser95=