Canonical Allele Identifier: CA2509358163
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152746_80152806del , CM000677.2:g.80152746_80152806del GRCh38
NC_000015.9:g.80445088_80445148del , CM000677.1:g.80445088_80445148del GRCh37
NC_000015.8:g.78232143_78232203del NCBI36
NG_012833.1:g.4748_4808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+201_-29-220del ENSP00000453152.1:n.-30+201_-29-220del