Canonical Allele Identifier: CA397005620
Gene: FOXF1 HGNC NCBI

Linked Data

COSMIC: COSM356037
MyVariant Identifiers: chr16:g.86544410C>A (hg19) chr16:g.86510804C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510804C>A , CM000678.2:g.86510804C>A GRCh38
NC_000016.9:g.86544410C>A , CM000678.1:g.86544410C>A GRCh37
NC_000016.8:g.85101911C>A NCBI36
NG_016273.1:g.5278C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.235C>A MANE Select ENSP00000262426.4:p.Gln79Lys
ENST00000262426.5:c.235C>A ENSP00000262426.4:p.Gln79Lys
NM_001451.2:c.235C>A NP_001442.2:p.Gln79Lys
NM_001451.3:c.235C>A MANE Select NP_001442.2:p.Gln79Lys
Search 100 bp 5'
Search 100 bp 3'