Canonical Allele Identifier: CA397005420
Gene: FOXF1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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