Canonical Allele Identifier: CA362558597
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610785T>G , CM000668.2:g.1610785T>G GRCh38
NC_000006.11:g.1611020T>G , CM000668.1:g.1611020T>G GRCh37
NC_000006.10:g.1556019T>G NCBI36
NG_009368.1:g.5340T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.340T>G MANE Select ENSP00000493906.1:p.Phe114Val
ENST00000380874.3:c.340T>G ENSP00000370256.2:p.Phe114Val
NM_001453.2:c.340T>G NP_001444.2:p.Phe114Val
NM_001453.3:c.340T>G MANE Select NP_001444.2:p.Phe114Val