Canonical Allele Identifier: CA397005856
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510858C>G , CM000678.2:g.86510858C>G GRCh38
NC_000016.9:g.86544464C>G , CM000678.1:g.86544464C>G GRCh37
NC_000016.8:g.85101965C>G NCBI36
NG_016273.1:g.5332C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.289C>G MANE Select ENSP00000262426.4:p.Arg97Gly
ENST00000262426.5:c.289C>G ENSP00000262426.4:p.Arg97Gly
NM_001451.2:c.289C>G NP_001442.2:p.Arg97Gly
NM_001451.3:c.289C>G MANE Select NP_001442.2:p.Arg97Gly