Canonical Allele Identifier: CA2677060951
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612484-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612484C>A , CM000668.2:g.1612484C>A GRCh38
NC_000006.11:g.1612719C>A , CM000668.1:g.1612719C>A GRCh37
NC_000006.10:g.1557718C>A NCBI36
NG_009368.1:g.7039C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*377C>A MANE Select ENSP00000493906.1:n.*377C>A
ENST00000380874.3:c.*377C>A ENSP00000370256.2:n.*377C>A
NM_001453.2:c.2039C>A NP_001444.2:n.2039C>A
NM_001453.3:c.*377C>A MANE Select NP_001444.2:n.*377C>A
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