Canonical Allele Identifier: CA497013671
Gene: FOXF1 HGNC NCBI

Linked Data

gnomAD v4: 16-86510701-G-C
MyVariant Identifiers: chr16:g.86544307G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510701G>C , CM000678.2:g.86510701G>C GRCh38
NC_000016.9:g.86544307G>C , CM000678.1:g.86544307G>C GRCh37
NC_000016.8:g.85101808G>C NCBI36
NG_016273.1:g.5175G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.132G>C MANE Select ENSP00000262426.4:p.Arg44=
ENST00000262426.5:c.132G>C ENSP00000262426.4:p.Arg44=
NM_001451.2:c.132G>C NP_001442.2:p.Arg44=
NM_001451.3:c.132G>C MANE Select NP_001442.2:p.Arg44=
Search 100 bp 5'
Search 100 bp 3'