Canonical Allele Identifier: CA2629872578
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152646_80152647insTGGCGGGGCGGGGGGAG , CM000677.2:g.80152646_80152647insTGGCGGGGCGGGGGGAG GRCh38
NC_000015.9:g.80444988_80444989insTGGCGGGGCGGGGGGAG , CM000677.1:g.80444988_80444989insTGGCGGGGCGGGGGGAG GRCh37
NC_000015.8:g.78232043_78232044insTGGCGGGGCGGGGGGAG NCBI36
NG_012833.1:g.4648_4649insTGGCGGGGCGGGGGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+101_-30+102insTGGCGGGGCGGGGGGAG ENSP00000453152.1:n.-30+101_-30+102insTGGCGGGGCGGGGGGAG