Canonical Allele Identifier: CA971894009
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152677_80152678insGGGGGGGC , CM000677.2:g.80152677_80152678insGGGGGGGC GRCh38
NC_000015.9:g.80445019_80445020insGGGGGGGC , CM000677.1:g.80445019_80445020insGGGGGGGC GRCh37
NC_000015.8:g.78232074_78232075insGGGGGGGC NCBI36
NG_012833.1:g.4679_4680insGGGGGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+132_-30+133insGGGGGGGC ENSP00000453152.1:n.-30+132_-30+133insGGGGGGGC