Canonical Allele Identifier: CA2502586808
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152674del , CM000677.2:g.80152674del GRCh38
NC_000015.9:g.80445016del , CM000677.1:g.80445016del GRCh37
NC_000015.8:g.78232071del NCBI36
NG_012833.1:g.4676del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+129del ENSP00000453152.1:n.-30+129del