Canonical Allele Identifier: CA2804914990
Gene: FAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152511_80152512insTTCGGGGG , CM000677.2:g.80152511_80152512insTTCGGGGG GRCh38
NC_000015.9:g.80444853_80444854insTTCGGGGG , CM000677.1:g.80444853_80444854insTTCGGGGG GRCh37
NC_000015.8:g.78231908_78231909insTTCGGGGG NCBI36
NG_012833.1:g.4513_4514insTTCGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-64_-63insTTCGGGGG ENSP00000453152.1:n.-64_-63insTTCGGGGG
Search 100 bp 5'
Search 100 bp 3'