Canonical Allele Identifier: CA2534971113
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152633dup , CM000677.2:g.80152633dup GRCh38
NC_000015.9:g.80444975dup , CM000677.1:g.80444975dup GRCh37
NC_000015.8:g.78232030dup NCBI36
NG_012833.1:g.4635dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+88dup ENSP00000453152.1:n.-30+88dup