Canonical Allele Identifier: CA8217367
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs768235643

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510755G>C , CM000678.2:g.86510755G>C GRCh38
NC_000016.9:g.86544361G>C , CM000678.1:g.86544361G>C GRCh37
NC_000016.8:g.85101862G>C NCBI36
NG_016273.1:g.5229G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.186G>C MANE Select ENSP00000262426.4:p.Gln62His
ENST00000262426.5:c.186G>C ENSP00000262426.4:p.Gln62His
NM_001451.2:c.186G>C NP_001442.2:p.Gln62His
NM_001451.3:c.186G>C MANE Select NP_001442.2:p.Gln62His