Canonical Allele Identifier: CA2516799887
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152768_80152836del , CM000677.2:g.80152768_80152836del GRCh38
NC_000015.9:g.80445110_80445178del , CM000677.1:g.80445110_80445178del GRCh37
NC_000015.8:g.78232165_78232233del NCBI36
NG_012833.1:g.4770_4838del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+223_-29-190del ENSP00000453152.1:n.-30+223_-29-190del