Canonical Allele Identifier: CA2677060968
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612502-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612502C>G , CM000668.2:g.1612502C>G GRCh38
NC_000006.11:g.1612737C>G , CM000668.1:g.1612737C>G GRCh37
NC_000006.10:g.1557736C>G NCBI36
NG_009368.1:g.7057C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*395C>G MANE Select ENSP00000493906.1:n.*395C>G
ENST00000380874.3:c.*395C>G ENSP00000370256.2:n.*395C>G
NM_001453.2:c.2057C>G NP_001444.2:n.2057C>G
NM_001453.3:c.*395C>G MANE Select NP_001444.2:n.*395C>G
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