Canonical Allele Identifier: CA2804915027
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152604_80152754del , CM000677.2:g.80152604_80152754del GRCh38
NC_000015.9:g.80444946_80445096del , CM000677.1:g.80444946_80445096del GRCh37
NC_000015.8:g.78232001_78232151del NCBI36
NG_012833.1:g.4606_4756del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+59_-30+209del ENSP00000453152.1:n.-30+59_-30+209del