Canonical Allele Identifier: CA821650164
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1476957589
gnomAD v3: 6-1612859-AATT-A
gnomAD v4: 6-1612859-AATT-A
MyVariant Identifiers: chr6:g.1613095_1613097del (hg19) chr6:g.1612860_1612862del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612864_1612866del , CM000668.2:g.1612864_1612866del GRCh38
NC_000006.11:g.1613099_1613101del , CM000668.1:g.1613099_1613101del GRCh37
NC_000006.10:g.1558098_1558100del NCBI36
NG_009368.1:g.7419_7421del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*757_*759del MANE Select ENSP00000493906.1:n.*757_*759del
ENST00000380874.3:c.*757_*759del ENSP00000370256.2:n.*757_*759del
NM_001453.2:c.2419_2421del NP_001444.2:n.2419_2421del
NM_001453.3:c.*757_*759del MANE Select NP_001444.2:n.*757_*759del
Search 100 bp 5'
Search 100 bp 3'