Canonical Allele Identifier: CA2804914991
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152508_80152527del , CM000677.2:g.80152508_80152527del GRCh38
NC_000015.9:g.80444850_80444869del , CM000677.1:g.80444850_80444869del GRCh37
NC_000015.8:g.78231905_78231924del NCBI36
NG_012833.1:g.4510_4529del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-67_-48del ENSP00000453152.1:n.-67_-48del