Canonical Allele Identifier: CA2629872552
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152644_80152645insGGGGGCGGGGCGAGGGG , CM000677.2:g.80152644_80152645insGGGGGCGGGGCGAGGGG GRCh38
NC_000015.9:g.80444986_80444987insGGGGGCGGGGCGAGGGG , CM000677.1:g.80444986_80444987insGGGGGCGGGGCGAGGGG GRCh37
NC_000015.8:g.78232041_78232042insGGGGGCGGGGCGAGGGG NCBI36
NG_012833.1:g.4646_4647insGGGGGCGGGGCGAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+99_-30+100insGGGGGCGGGGCGAGGGG ENSP00000453152.1:n.-30+99_-30+100insGGGGGCGGGGCGAGGGG