Canonical Allele Identifier: CA971893264

Gene: FAH

Linked Data

• dbSNP Id: rs1595888206
• gnomAD v3: 15-80152528-A-G
• gnomAD v4: 15-80152528-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152528A>G , CM000677.2:g.80152528A>G	GRCh38
NC_000015.9:g.80444870A>G , CM000677.1:g.80444870A>G	GRCh37
NC_000015.8:g.78231925A>G	NCBI36
NG_012833.1:g.4530A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-47A>G	ENSP00000453152.1:n.-47A>G