Canonical Allele Identifier: CA397005617
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544408T>C (hg19) chr16:g.86510802T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510802T>C , CM000678.2:g.86510802T>C GRCh38
NC_000016.9:g.86544408T>C , CM000678.1:g.86544408T>C GRCh37
NC_000016.8:g.85101909T>C NCBI36
NG_016273.1:g.5276T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.233T>C MANE Select ENSP00000262426.4:p.Leu78Pro
ENST00000262426.5:c.233T>C ENSP00000262426.4:p.Leu78Pro
NM_001451.2:c.233T>C NP_001442.2:p.Leu78Pro
NM_001451.3:c.233T>C MANE Select NP_001442.2:p.Leu78Pro
Search 100 bp 5'
Search 100 bp 3'