Canonical Allele Identifier: CA397005887
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544471A>G (hg19) chr16:g.86510865A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510865A>G , CM000678.2:g.86510865A>G GRCh38
NC_000016.9:g.86544471A>G , CM000678.1:g.86544471A>G GRCh37
NC_000016.8:g.85101972A>G NCBI36
NG_016273.1:g.5339A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.296A>G MANE Select ENSP00000262426.4:p.Asn99Ser
ENST00000262426.5:c.296A>G ENSP00000262426.4:p.Asn99Ser
NM_001451.2:c.296A>G NP_001442.2:p.Asn99Ser
NM_001451.3:c.296A>G MANE Select NP_001442.2:p.Asn99Ser
Search 100 bp 5'
Search 100 bp 3'