Canonical Allele Identifier: CA497013799
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs1319217979

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510866C>T , CM000678.2:g.86510866C>T GRCh38
NC_000016.9:g.86544472C>T , CM000678.1:g.86544472C>T GRCh37
NC_000016.8:g.85101973C>T NCBI36
NG_016273.1:g.5340C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262426.6:c.297C>T MANE Select ENSP00000262426.4:p.Asn99=
ENST00000262426.5:c.297C>T ENSP00000262426.4:p.Asn99=
NM_001451.2:c.297C>T NP_001442.2:p.Asn99=
NM_001451.3:c.297C>T MANE Select NP_001442.2:p.Asn99=