Canonical Allele Identifier: CA2629872421

Gene: FAH

Linked Data

• gnomAD v4: 15-80152494-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152494G>T , CM000677.2:g.80152494G>T	GRCh38
NC_000015.9:g.80444836G>T , CM000677.1:g.80444836G>T	GRCh37
NC_000015.8:g.78231891G>T	NCBI36
NG_012833.1:g.4496G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-81G>T	ENSP00000453152.1:n.-81G>T