Canonical Allele Identifier: CA971893254

Gene: FAH

Linked Data

• gnomAD v3: 15-80152524-C-CTG
• gnomAD v4: 15-80152524-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152525_80152526dup , CM000677.2:g.80152525_80152526dup	GRCh38
NC_000015.9:g.80444867_80444868dup , CM000677.1:g.80444867_80444868dup	GRCh37
NC_000015.8:g.78231922_78231923dup	NCBI36
NG_012833.1:g.4527_4528dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-50_-49dup	ENSP00000453152.1:n.-50_-49dup