Canonical Allele Identifier: CA2629872545
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152637_80152638insGGAGGGGAGGGGCGGGG , CM000677.2:g.80152637_80152638insGGAGGGGAGGGGCGGGG GRCh38
NC_000015.9:g.80444979_80444980insGGAGGGGAGGGGCGGGG , CM000677.1:g.80444979_80444980insGGAGGGGAGGGGCGGGG GRCh37
NC_000015.8:g.78232034_78232035insGGAGGGGAGGGGCGGGG NCBI36
NG_012833.1:g.4639_4640insGGAGGGGAGGGGCGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+92_-30+93insGGAGGGGAGGGGCGGGG ENSP00000453152.1:n.-30+92_-30+93insGGAGGGGAGGGGCGGGG