Canonical Allele Identifier: CA2629872432
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152504_80152505insGAGGCTTGTGCCATTTTT , CM000677.2:g.80152504_80152505insGAGGCTTGTGCCATTTTT GRCh38
NC_000015.9:g.80444846_80444847insGAGGCTTGTGCCATTTTT , CM000677.1:g.80444846_80444847insGAGGCTTGTGCCATTTTT GRCh37
NC_000015.8:g.78231901_78231902insGAGGCTTGTGCCATTTTT NCBI36
NG_012833.1:g.4506_4507insGAGGCTTGTGCCATTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-71_-70insGAGGCTTGTGCCATTTTT ENSP00000453152.1:n.-71_-70insGAGGCTTGTGCCATTTTT