Canonical Allele Identifier: CA212544
Gene: FOXF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190130
ClinVar RCV Id: RCV000201858
dbSNP Id: rs752504125
MyVariant Identifiers: chr16:g.86544833G>T (hg19) chr16:g.86511227G>T (hg38)
PubMed: PMID:2629409 PMID:26294094
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86511227G>T , CM000678.2:g.86511227G>T GRCh38
NC_000016.9:g.86544833G>T , CM000678.1:g.86544833G>T GRCh37
NC_000016.8:g.85102334G>T NCBI36
NG_016273.1:g.5701G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262426.6:c.658G>T MANE Select ENSP00000262426.4:p.Gly220Cys
ENST00000262426.5:c.658G>T ENSP00000262426.4:p.Gly220Cys
NM_001451.2:c.658G>T NP_001442.2:p.Gly220Cys
NM_001451.3:c.658G>T MANE Select NP_001442.2:p.Gly220Cys
Search 100 bp 5'
Search 100 bp 3'