Canonical Allele Identifier: CA397005874
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510862A>G , CM000678.2:g.86510862A>G GRCh38
NC_000016.9:g.86544468A>G , CM000678.1:g.86544468A>G GRCh37
NC_000016.8:g.85101969A>G NCBI36
NG_016273.1:g.5336A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.293A>G MANE Select ENSP00000262426.4:p.His98Arg
ENST00000262426.5:c.293A>G ENSP00000262426.4:p.His98Arg
NM_001451.2:c.293A>G NP_001442.2:p.His98Arg
NM_001451.3:c.293A>G MANE Select NP_001442.2:p.His98Arg