Canonical Allele Identifier: CA497013679
Gene: FOXF1 HGNC NCBI

Linked Data

gnomAD v4: 16-86510707-G-C
MyVariant Identifiers: chr16:g.86544313G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510707G>C , CM000678.2:g.86510707G>C GRCh38
NC_000016.9:g.86544313G>C , CM000678.1:g.86544313G>C GRCh37
NC_000016.8:g.85101814G>C NCBI36
NG_016273.1:g.5181G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.138G>C MANE Select ENSP00000262426.4:p.Pro46=
ENST00000262426.5:c.138G>C ENSP00000262426.4:p.Pro46=
NM_001451.2:c.138G>C NP_001442.2:p.Pro46=
NM_001451.3:c.138G>C MANE Select NP_001442.2:p.Pro46=
Search 100 bp 5'
Search 100 bp 3'