Canonical Allele Identifier: CA2804914983
Gene: FAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152492_80152493insCCT , CM000677.2:g.80152492_80152493insCCT GRCh38
NC_000015.9:g.80444834_80444835insCCT , CM000677.1:g.80444834_80444835insCCT GRCh37
NC_000015.8:g.78231889_78231890insCCT NCBI36
NG_012833.1:g.4494_4495insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-83_-82insCCT ENSP00000453152.1:n.-83_-82insCCT
Search 100 bp 5'
Search 100 bp 3'