Canonical Allele Identifier: CA2190327008
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152641_80152658delinsGGGGAGGGGCGGGGCTCA , CM000677.2:g.80152641_80152658delinsGGGGAGGGGCGGGGCTCA GRCh38
NC_000015.9:g.80444983_80445000delinsGGGGAGGGGCGGGGCTCA , CM000677.1:g.80444983_80445000delinsGGGGAGGGGCGGGGCTCA GRCh37
NC_000015.8:g.78232038_78232055delinsGGGGAGGGGCGGGGCTCA NCBI36
NG_012833.1:g.4643_4660delinsGGGGAGGGGCGGGGCTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+96_-30+113delinsGGGGAGGGGCGGGGCTCA ENSP00000453152.1:n.-30+96_-30+113delinsGGGGAGGGGCGGGGCTCA