Canonical Allele Identifier: CA2677061178
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1613042-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613042A>G , CM000668.2:g.1613042A>G GRCh38
NC_000006.11:g.1613277A>G , CM000668.1:g.1613277A>G GRCh37
NC_000006.10:g.1558276A>G NCBI36
NG_009368.1:g.7597A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*935A>G MANE Select ENSP00000493906.1:n.*935A>G
ENST00000380874.3:c.*935A>G ENSP00000370256.2:n.*935A>G
NM_001453.2:c.2597A>G NP_001444.2:n.2597A>G
NM_001453.3:c.*935A>G MANE Select NP_001444.2:n.*935A>G
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