Canonical Allele Identifier: CA397005871
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544468A>C (hg19) chr16:g.86510862A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510862A>C , CM000678.2:g.86510862A>C GRCh38
NC_000016.9:g.86544468A>C , CM000678.1:g.86544468A>C GRCh37
NC_000016.8:g.85101969A>C NCBI36
NG_016273.1:g.5336A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.293A>C MANE Select ENSP00000262426.4:p.His98Pro
ENST00000262426.5:c.293A>C ENSP00000262426.4:p.His98Pro
NM_001451.2:c.293A>C NP_001442.2:p.His98Pro
NM_001451.3:c.293A>C MANE Select NP_001442.2:p.His98Pro
Search 100 bp 5'
Search 100 bp 3'