Canonical Allele Identifier: CA2190326956
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152626G= , CM000677.2:g.80152626G= GRCh38
NC_000015.9:g.80444968G= , CM000677.1:g.80444968G= GRCh37
NC_000015.8:g.78232023G= NCBI36
NG_012833.1:g.4628G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+81G= ENSP00000453152.1:n.-30+81G=