Canonical Allele Identifier: CA619266156
Gene: FAH HGNC NCBI

Linked Data

gnomAD v2: 15-80445000-A-AGGGGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAG
gnomAD v3: 15-80152658-A-AGGGGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAG
gnomAD v4: 15-80152658-A-AGGGGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAG
MyVariant Identifiers: chr15:g.80445000_80445001insGGGGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAG (hg19) chr15:g.80152658_80152659insGGGGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152661_80152662insGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAGGGG , CM000677.2:g.80152661_80152662insGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAGGGG GRCh38
NC_000015.9:g.80445003_80445004insGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAGGGG , CM000677.1:g.80445003_80445004insGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAGGGG GRCh37
NC_000015.8:g.78232058_78232059insGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAGGGG NCBI36
NG_012833.1:g.4663_4664insGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+116_-30+117insGAGGGGCGGGGCGAGGGGAGGGGCGGGGCGAGGGG ENSP00000453152.1:n.-30+116_-30+117insGAGGGGCGGGGCGAGGGGAGGGG...
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