Canonical Allele Identifier: CA2804914993
Gene: FAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152508_80152509insTTCC , CM000677.2:g.80152508_80152509insTTCC GRCh38
NC_000015.9:g.80444850_80444851insTTCC , CM000677.1:g.80444850_80444851insTTCC GRCh37
NC_000015.8:g.78231905_78231906insTTCC NCBI36
NG_012833.1:g.4510_4511insTTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-67_-66insTTCC ENSP00000453152.1:n.-67_-66insTTCC
Search 100 bp 5'
Search 100 bp 3'