Canonical Allele Identifier: CA2804915055
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152639_80152640insGTGAGACCAAA , CM000677.2:g.80152639_80152640insGTGAGACCAAA GRCh38
NC_000015.9:g.80444981_80444982insGTGAGACCAAA , CM000677.1:g.80444981_80444982insGTGAGACCAAA GRCh37
NC_000015.8:g.78232036_78232037insGTGAGACCAAA NCBI36
NG_012833.1:g.4641_4642insGTGAGACCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+94_-30+95insGTGAGACCAAA ENSP00000453152.1:n.-30+94_-30+95insGTGAGACCAAA