Canonical Allele Identifier: CA397005457
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510763C>G , CM000678.2:g.86510763C>G GRCh38
NC_000016.9:g.86544369C>G , CM000678.1:g.86544369C>G GRCh37
NC_000016.8:g.85101870C>G NCBI36
NG_016273.1:g.5237C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.194C>G MANE Select ENSP00000262426.4:p.Pro65Arg
ENST00000262426.5:c.194C>G ENSP00000262426.4:p.Pro65Arg
NM_001451.2:c.194C>G NP_001442.2:p.Pro65Arg
NM_001451.3:c.194C>G MANE Select NP_001442.2:p.Pro65Arg