Canonical Allele Identifier: CA8217370
Gene: FOXF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320789
ClinVar RCV Id: RCV000891033
dbSNP Id: rs370422274
ExAC: 16:86544379 C / G
gnomAD v2: 16-86544379-C-G
gnomAD v3: 16-86510773-C-G
gnomAD v4: 16-86510773-C-G
MyVariant Identifiers: chr16:g.86544379C>G (hg19) chr16:g.86510773C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510773C>G , CM000678.2:g.86510773C>G GRCh38
NC_000016.9:g.86544379C>G , CM000678.1:g.86544379C>G GRCh37
NC_000016.8:g.85101880C>G NCBI36
NG_016273.1:g.5247C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262426.6:c.204C>G MANE Select ENSP00000262426.4:p.Arg68=
ENST00000262426.5:c.204C>G ENSP00000262426.4:p.Arg68=
NM_001451.2:c.204C>G NP_001442.2:p.Arg68=
NM_001451.3:c.204C>G MANE Select NP_001442.2:p.Arg68=
Search 100 bp 5'
Search 100 bp 3'