Canonical Allele Identifier: CA2804915007
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152554del , CM000677.2:g.80152554del GRCh38
NC_000015.9:g.80444896del , CM000677.1:g.80444896del GRCh37
NC_000015.8:g.78231951del NCBI36
NG_012833.1:g.4556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+9del ENSP00000453152.1:n.-30+9del