Canonical Allele Identifier: CA2629872645

Gene: FAH

Linked Data

• gnomAD v4: 15-80152666-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152669dup , CM000677.2:g.80152669dup	GRCh38
NC_000015.9:g.80445011dup , CM000677.1:g.80445011dup	GRCh37
NC_000015.8:g.78232066dup	NCBI36
NG_012833.1:g.4671dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-30+124dup	ENSP00000453152.1:n.-30+124dup