Canonical Allele Identifier: CA2677061066
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612745-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612745C>A , CM000668.2:g.1612745C>A GRCh38
NC_000006.11:g.1612980C>A , CM000668.1:g.1612980C>A GRCh37
NC_000006.10:g.1557979C>A NCBI36
NG_009368.1:g.7300C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*638C>A MANE Select ENSP00000493906.1:n.*638C>A
ENST00000380874.3:c.*638C>A ENSP00000370256.2:n.*638C>A
NM_001453.2:c.2300C>A NP_001444.2:n.2300C>A
NM_001453.3:c.*638C>A MANE Select NP_001444.2:n.*638C>A
Search 100 bp 5'
Search 100 bp 3'