Canonical Allele Identifier: CA1605822035
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610117G= , CM000668.2:g.1610117G= GRCh38
NC_000006.11:g.1610352G= , CM000668.1:g.1610352G= GRCh37
NC_000006.10:g.1555351G= NCBI36
NG_009368.1:g.4672G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-329G= MANE Select ENSP00000493906.1:n.-329G=
ENST00000380874.3:c.-329G= ENSP00000370256.2:n.-329G=
NM_001453.3:c.-329G= MANE Select NP_001444.2:n.-329G=
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