Canonical Allele Identifier: CA397005832
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs1272343929

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.283T>A MANE Select ENSP00000262426.4:p.Ser95Thr
ENST00000262426.5:c.283T>A ENSP00000262426.4:p.Ser95Thr
NM_001451.2:c.283T>A NP_001442.2:p.Ser95Thr
NM_001451.3:c.283T>A MANE Select NP_001442.2:p.Ser95Thr