Canonical Allele Identifier: CA971893991
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152673_80152674insGGGGGGGGGG , CM000677.2:g.80152673_80152674insGGGGGGGGGG GRCh38
NC_000015.9:g.80445015_80445016insGGGGGGGGGG , CM000677.1:g.80445015_80445016insGGGGGGGGGG GRCh37
NC_000015.8:g.78232070_78232071insGGGGGGGGGG NCBI36
NG_012833.1:g.4675_4676insGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+128_-30+129insGGGGGGGGGG ENSP00000453152.1:n.-30+128_-30+129insGGGGGGGGGG