Canonical Allele Identifier: CA2677061195
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1613083-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613083C>T , CM000668.2:g.1613083C>T GRCh38
NC_000006.11:g.1613318C>T , CM000668.1:g.1613318C>T GRCh37
NC_000006.10:g.1558317C>T NCBI36
NG_009368.1:g.7638C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*976C>T MANE Select ENSP00000493906.1:n.*976C>T
ENST00000380874.3:c.*976C>T ENSP00000370256.2:n.*976C>T
NM_001453.2:c.2638C>T NP_001444.2:n.2638C>T
NM_001453.3:c.*976C>T MANE Select NP_001444.2:n.*976C>T
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