Canonical Allele Identifier: CA2629872581
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152643G>A , CM000677.2:g.80152643G>A GRCh38
NC_000015.9:g.80444985G>A , CM000677.1:g.80444985G>A GRCh37
NC_000015.8:g.78232040G>A NCBI36
NG_012833.1:g.4645G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+98G>A ENSP00000453152.1:n.-30+98G>A