Canonical Allele Identifier: CA971893727
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152641_80152644del , CM000677.2:g.80152641_80152644del GRCh38
NC_000015.9:g.80444983_80444986del , CM000677.1:g.80444983_80444986del GRCh37
NC_000015.8:g.78232038_78232041del NCBI36
NG_012833.1:g.4643_4646del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+96_-30+99del ENSP00000453152.1:n.-30+96_-30+99del