Canonical Allele Identifier: CA497013667
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544305C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510699C>A , CM000678.2:g.86510699C>A GRCh38
NC_000016.9:g.86544305C>A , CM000678.1:g.86544305C>A GRCh37
NC_000016.8:g.85101806C>A NCBI36
NG_016273.1:g.5173C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.130C>A MANE Select ENSP00000262426.4:p.Arg44=
ENST00000262426.5:c.130C>A ENSP00000262426.4:p.Arg44=
NM_001451.2:c.130C>A NP_001442.2:p.Arg44=
NM_001451.3:c.130C>A MANE Select NP_001442.2:p.Arg44=
Search 100 bp 5'
Search 100 bp 3'