Canonical Allele Identifier: CA1605822299
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610442G= , CM000668.2:g.1610442G= GRCh38
NC_000006.11:g.1610677G= , CM000668.1:g.1610677G= GRCh37
NC_000006.10:g.1555676G= NCBI36
NG_009368.1:g.4997G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-4G= MANE Select ENSP00000493906.1:n.-4G=
ENST00000380874.3:c.-4G= ENSP00000370256.2:n.-4G=
NM_001453.3:c.-4G= MANE Select NP_001444.2:n.-4G=
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