Canonical Allele Identifier: CA971893492
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152583A>G , CM000677.2:g.80152583A>G GRCh38
NC_000015.9:g.80444925A>G , CM000677.1:g.80444925A>G GRCh37
NC_000015.8:g.78231980A>G NCBI36
NG_012833.1:g.4585A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+38A>G ENSP00000453152.1:n.-30+38A>G