Canonical Allele Identifier: CA2677061117
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612919-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612919A>C , CM000668.2:g.1612919A>C GRCh38
NC_000006.11:g.1613154A>C , CM000668.1:g.1613154A>C GRCh37
NC_000006.10:g.1558153A>C NCBI36
NG_009368.1:g.7474A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*812A>C MANE Select ENSP00000493906.1:n.*812A>C
ENST00000380874.3:c.*812A>C ENSP00000370256.2:n.*812A>C
NM_001453.2:c.2474A>C NP_001444.2:n.2474A>C
NM_001453.3:c.*812A>C MANE Select NP_001444.2:n.*812A>C
Search 100 bp 5'
Search 100 bp 3'