Canonical Allele Identifier: CA397005307
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs1969548058
gnomAD v3: 16-86510705-C-T
gnomAD v4: 16-86510705-C-T
MyVariant Identifiers: chr16:g.86544311C>T (hg19) chr16:g.86510705C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510705C>T , CM000678.2:g.86510705C>T GRCh38
NC_000016.9:g.86544311C>T , CM000678.1:g.86544311C>T GRCh37
NC_000016.8:g.85101812C>T NCBI36
NG_016273.1:g.5179C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.136C>T MANE Select ENSP00000262426.4:p.Pro46Ser
ENST00000262426.5:c.136C>T ENSP00000262426.4:p.Pro46Ser
NM_001451.2:c.136C>T NP_001442.2:p.Pro46Ser
NM_001451.3:c.136C>T MANE Select NP_001442.2:p.Pro46Ser
Search 100 bp 5'
Search 100 bp 3'