Canonical Allele Identifier: CA2629872456

Gene: FAH

Linked Data

• gnomAD v4: 15-80152533-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152533C>T , CM000677.2:g.80152533C>T	GRCh38
NC_000015.9:g.80444875C>T , CM000677.1:g.80444875C>T	GRCh37
NC_000015.8:g.78231930C>T	NCBI36
NG_012833.1:g.4535C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-42C>T	ENSP00000453152.1:n.-42C>T