Canonical Allele Identifier: CA397005889
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544472C>A (hg19) chr16:g.86510866C>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.297C>A MANE Select ENSP00000262426.4:p.Asn99Lys
ENST00000262426.5:c.297C>A ENSP00000262426.4:p.Asn99Lys
NM_001451.2:c.297C>A NP_001442.2:p.Asn99Lys
NM_001451.3:c.297C>A MANE Select NP_001442.2:p.Asn99Lys
Search 100 bp 5'
Search 100 bp 3'