Canonical Allele Identifier: CA2629872623
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152661_80152662insGAGGGCGGGGCGAGGGG , CM000677.2:g.80152661_80152662insGAGGGCGGGGCGAGGGG GRCh38
NC_000015.9:g.80445003_80445004insGAGGGCGGGGCGAGGGG , CM000677.1:g.80445003_80445004insGAGGGCGGGGCGAGGGG GRCh37
NC_000015.8:g.78232058_78232059insGAGGGCGGGGCGAGGGG NCBI36
NG_012833.1:g.4663_4664insGAGGGCGGGGCGAGGGG

Transcript Alleles

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