Canonical Allele Identifier: CA2804914985
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152505_80152506insCGGGCCTGACCACAGCGGCCGAGT , CM000677.2:g.80152505_80152506insCGGGCCTGACCACAGCGGCCGAGT GRCh38
NC_000015.9:g.80444847_80444848insCGGGCCTGACCACAGCGGCCGAGT , CM000677.1:g.80444847_80444848insCGGGCCTGACCACAGCGGCCGAGT GRCh37
NC_000015.8:g.78231902_78231903insCGGGCCTGACCACAGCGGCCGAGT NCBI36
NG_012833.1:g.4507_4508insCGGGCCTGACCACAGCGGCCGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-70_-69insCGGGCCTGACCACAGCGGCCGAGT ENSP00000453152.1:n.-70_-69insCGGGCCTGACCACAGCGGCCGAGT