Canonical Allele Identifier: CA397005411
Gene: FOXF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630000
ClinVar RCV Id: RCV003391308
MyVariant Identifiers: chr16:g.86544357T>C (hg19) chr16:g.86510751T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510751T>C , CM000678.2:g.86510751T>C GRCh38
NC_000016.9:g.86544357T>C , CM000678.1:g.86544357T>C GRCh37
NC_000016.8:g.85101858T>C NCBI36
NG_016273.1:g.5225T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.182T>C MANE Select ENSP00000262426.4:p.Ile61Thr
ENST00000262426.5:c.182T>C ENSP00000262426.4:p.Ile61Thr
NM_001451.2:c.182T>C NP_001442.2:p.Ile61Thr
NM_001451.3:c.182T>C MANE Select NP_001442.2:p.Ile61Thr
Search 100 bp 5'
Search 100 bp 3'