Canonical Allele Identifier: CA2677060939
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612472-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612472C>A , CM000668.2:g.1612472C>A GRCh38
NC_000006.11:g.1612707C>A , CM000668.1:g.1612707C>A GRCh37
NC_000006.10:g.1557706C>A NCBI36
NG_009368.1:g.7027C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*365C>A MANE Select ENSP00000493906.1:n.*365C>A
ENST00000380874.3:c.*365C>A ENSP00000370256.2:n.*365C>A
NM_001453.2:c.2027C>A NP_001444.2:n.2027C>A
NM_001453.3:c.*365C>A MANE Select NP_001444.2:n.*365C>A
Search 100 bp 5'
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