Canonical Allele Identifier: CA397005407
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510750A>C , CM000678.2:g.86510750A>C GRCh38
NC_000016.9:g.86544356A>C , CM000678.1:g.86544356A>C GRCh37
NC_000016.8:g.85101857A>C NCBI36
NG_016273.1:g.5224A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.181A>C MANE Select ENSP00000262426.4:p.Ile61Leu
ENST00000262426.5:c.181A>C ENSP00000262426.4:p.Ile61Leu
NM_001451.2:c.181A>C NP_001442.2:p.Ile61Leu
NM_001451.3:c.181A>C MANE Select NP_001442.2:p.Ile61Leu