Canonical Allele Identifier: CA8217368
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs774031341

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510766C>T , CM000678.2:g.86510766C>T GRCh38
NC_000016.9:g.86544372C>T , CM000678.1:g.86544372C>T GRCh37
NC_000016.8:g.85101873C>T NCBI36
NG_016273.1:g.5240C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262426.6:c.197C>T MANE Select ENSP00000262426.4:p.Thr66Ile
ENST00000262426.5:c.197C>T ENSP00000262426.4:p.Thr66Ile
NM_001451.2:c.197C>T NP_001442.2:p.Thr66Ile
NM_001451.3:c.197C>T MANE Select NP_001442.2:p.Thr66Ile