Canonical Allele Identifier: CA2536282616
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152492_80152493insCCTGACCACAGC , CM000677.2:g.80152492_80152493insCCTGACCACAGC GRCh38
NC_000015.9:g.80444834_80444835insCCTGACCACAGC , CM000677.1:g.80444834_80444835insCCTGACCACAGC GRCh37
NC_000015.8:g.78231889_78231890insCCTGACCACAGC NCBI36
NG_012833.1:g.4494_4495insCCTGACCACAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-83_-82insCCTGACCACAGC ENSP00000453152.1:n.-83_-82insCCTGACCACAGC