Canonical Allele Identifier: CA397005288
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544302A>G (hg19) chr16:g.86510696A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510696A>G , CM000678.2:g.86510696A>G GRCh38
NC_000016.9:g.86544302A>G , CM000678.1:g.86544302A>G GRCh37
NC_000016.8:g.85101803A>G NCBI36
NG_016273.1:g.5170A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.127A>G MANE Select ENSP00000262426.4:p.Ile43Val
ENST00000262426.5:c.127A>G ENSP00000262426.4:p.Ile43Val
NM_001451.2:c.127A>G NP_001442.2:p.Ile43Val
NM_001451.3:c.127A>G MANE Select NP_001442.2:p.Ile43Val
Search 100 bp 5'
Search 100 bp 3'