Canonical Allele Identifier: CA821645757
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1192019316
gnomAD v3: 6-1610406-G-GGGGGCGGCGGGCGGCGC
gnomAD v4: 6-1610406-G-GGGGGCGGCGGGCGGCGC
MyVariant Identifiers: chr6:g.1610641_1610642insGGGGCGGCGGGCGGCGC (hg19) chr6:g.1610406_1610407insGGGGCGGCGGGCGGCGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610417_1610433dup , CM000668.2:g.1610417_1610433dup GRCh38
NC_000006.11:g.1610652_1610668dup , CM000668.1:g.1610652_1610668dup GRCh37
NC_000006.10:g.1555651_1555667dup NCBI36
NG_009368.1:g.4972_4988dup

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-29_-13dup MANE Select ENSP00000493906.1:n.-29_-13dup
ENST00000380874.3:c.-29_-13dup ENSP00000370256.2:n.-29_-13dup
NM_001453.3:c.-29_-13dup MANE Select NP_001444.2:n.-29_-13dup
Search 100 bp 5'
Search 100 bp 3'