Canonical Allele Identifier: CA397005447
Gene: FOXF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 800369
ClinVar RCV Id: RCV000984337
dbSNP Id: rs1597291235
MyVariant Identifiers: chr16:g.86544366C>A (hg19) chr16:g.86510760C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510760C>A , CM000678.2:g.86510760C>A GRCh38
NC_000016.9:g.86544366C>A , CM000678.1:g.86544366C>A GRCh37
NC_000016.8:g.85101867C>A NCBI36
NG_016273.1:g.5234C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.191C>A MANE Select ENSP00000262426.4:p.Ser64Ter
ENST00000262426.5:c.191C>A ENSP00000262426.4:p.Ser64Ter
NM_001451.2:c.191C>A NP_001442.2:p.Ser64Ter
NM_001451.3:c.191C>A MANE Select NP_001442.2:p.Ser64Ter
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