Canonical Allele Identifier: CA1605822478
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610742C= , CM000668.2:g.1610742C= GRCh38
NC_000006.11:g.1610977C= , CM000668.1:g.1610977C= GRCh37
NC_000006.10:g.1555976C= NCBI36
NG_009368.1:g.5297C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.297C= MANE Select ENSP00000493906.1:p.Ile99=
ENST00000380874.3:c.297C= ENSP00000370256.2:p.Ile99=
NM_001453.2:c.297C= NP_001444.2:p.Ile99=
NM_001453.3:c.297C= MANE Select NP_001444.2:p.Ile99=
Search 100 bp 5'
Search 100 bp 3'