Canonical Allele Identifier: CA1605822297
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610440G= , CM000668.2:g.1610440G= GRCh38
NC_000006.11:g.1610675G= , CM000668.1:g.1610675G= GRCh37
NC_000006.10:g.1555674G= NCBI36
NG_009368.1:g.4995G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-6G= MANE Select ENSP00000493906.1:n.-6G=
ENST00000380874.3:c.-6G= ENSP00000370256.2:n.-6G=
NM_001453.3:c.-6G= MANE Select NP_001444.2:n.-6G=
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