Canonical Allele Identifier: CA397005604
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544405T>G (hg19) chr16:g.86510799T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510799T>G , CM000678.2:g.86510799T>G GRCh38
NC_000016.9:g.86544405T>G , CM000678.1:g.86544405T>G GRCh37
NC_000016.8:g.85101906T>G NCBI36
NG_016273.1:g.5273T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.230T>G MANE Select ENSP00000262426.4:p.Phe77Cys
ENST00000262426.5:c.230T>G ENSP00000262426.4:p.Phe77Cys
NM_001451.2:c.230T>G NP_001442.2:p.Phe77Cys
NM_001451.3:c.230T>G MANE Select NP_001442.2:p.Phe77Cys
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