Canonical Allele Identifier: CA397005897
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544473C>A (hg19) chr16:g.86510867C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510867C>A , CM000678.2:g.86510867C>A GRCh38
NC_000016.9:g.86544473C>A , CM000678.1:g.86544473C>A GRCh37
NC_000016.8:g.85101974C>A NCBI36
NG_016273.1:g.5341C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.298C>A MANE Select ENSP00000262426.4:p.Leu100Ile
ENST00000262426.5:c.298C>A ENSP00000262426.4:p.Leu100Ile
NM_001451.2:c.298C>A NP_001442.2:p.Leu100Ile
NM_001451.3:c.298C>A MANE Select NP_001442.2:p.Leu100Ile
Search 100 bp 5'
Search 100 bp 3'