Canonical Allele Identifier: CA2629872575
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152654_80152655insGGAGGGGAGGGGCGGGG , CM000677.2:g.80152654_80152655insGGAGGGGAGGGGCGGGG GRCh38
NC_000015.9:g.80444996_80444997insGGAGGGGAGGGGCGGGG , CM000677.1:g.80444996_80444997insGGAGGGGAGGGGCGGGG GRCh37
NC_000015.8:g.78232051_78232052insGGAGGGGAGGGGCGGGG NCBI36
NG_012833.1:g.4656_4657insGGAGGGGAGGGGCGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+109_-30+110insGGAGGGGAGGGGCGGGG ENSP00000453152.1:n.-30+109_-30+110insGGAGGGGAGGGGCGGGG