Canonical Allele Identifier: CA156260
Gene: FOXF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 132838
ClinVar RCV Id: RCV000119307
dbSNP Id: rs672601295
MyVariant Identifiers: chr16:g.86544591G>A (hg19) chr16:g.86510985G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510985G>A , CM000678.2:g.86510985G>A GRCh38
NC_000016.9:g.86544591G>A , CM000678.1:g.86544591G>A GRCh37
NC_000016.8:g.85102092G>A NCBI36
NG_016273.1:g.5459G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262426.6:c.416G>A MANE Select ENSP00000262426.4:p.Arg139Gln
ENST00000262426.5:c.416G>A ENSP00000262426.4:p.Arg139Gln
NM_001451.2:c.416G>A NP_001442.2:p.Arg139Gln
NM_001451.3:c.416G>A MANE Select NP_001442.2:p.Arg139Gln
Search 100 bp 5'
Search 100 bp 3'