Canonical Allele Identifier: CA2804914981
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152494_80152499del , CM000677.2:g.80152494_80152499del GRCh38
NC_000015.9:g.80444836_80444841del , CM000677.1:g.80444836_80444841del GRCh37
NC_000015.8:g.78231891_78231896del NCBI36
NG_012833.1:g.4496_4501del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-81_-76del ENSP00000453152.1:n.-81_-76del