Canonical Allele Identifier: CA397005627
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs1969549778
MyVariant Identifiers: chr16:g.86544411A>G (hg19) chr16:g.86510805A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510805A>G , CM000678.2:g.86510805A>G GRCh38
NC_000016.9:g.86544411A>G , CM000678.1:g.86544411A>G GRCh37
NC_000016.8:g.85101912A>G NCBI36
NG_016273.1:g.5279A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.236A>G MANE Select ENSP00000262426.4:p.Gln79Arg
ENST00000262426.5:c.236A>G ENSP00000262426.4:p.Gln79Arg
NM_001451.2:c.236A>G NP_001442.2:p.Gln79Arg
NM_001451.3:c.236A>G MANE Select NP_001442.2:p.Gln79Arg
Search 100 bp 5'
Search 100 bp 3'