Canonical Allele Identifier: CA2731281638

Gene: FAH

Linked Data

• dbSNP Id: rs1487645227

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152495A>T , CM000677.2:g.80152495A>T	GRCh38
NC_000015.9:g.80444837A>T , CM000677.1:g.80444837A>T	GRCh37
NC_000015.8:g.78231892A>T	NCBI36
NG_012833.1:g.4497A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-80A>T	ENSP00000453152.1:n.-80A>T