Canonical Allele Identifier: CA397005862
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510859G>C , CM000678.2:g.86510859G>C GRCh38
NC_000016.9:g.86544465G>C , CM000678.1:g.86544465G>C GRCh37
NC_000016.8:g.85101966G>C NCBI36
NG_016273.1:g.5333G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.290G>C MANE Select ENSP00000262426.4:p.Arg97Pro
ENST00000262426.5:c.290G>C ENSP00000262426.4:p.Arg97Pro
NM_001451.2:c.290G>C NP_001442.2:p.Arg97Pro
NM_001451.3:c.290G>C MANE Select NP_001442.2:p.Arg97Pro