Canonical Allele Identifier: CA2629872539
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152622_80152623insGGGGGAGGGGCGGGGCG , CM000677.2:g.80152622_80152623insGGGGGAGGGGCGGGGCG GRCh38
NC_000015.9:g.80444964_80444965insGGGGGAGGGGCGGGGCG , CM000677.1:g.80444964_80444965insGGGGGAGGGGCGGGGCG GRCh37
NC_000015.8:g.78232019_78232020insGGGGGAGGGGCGGGGCG NCBI36
NG_012833.1:g.4624_4625insGGGGGAGGGGCGGGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+77_-30+78insGGGGGAGGGGCGGGGCG ENSP00000453152.1:n.-30+77_-30+78insGGGGGAGGGGCGGGGCG