Canonical Allele Identifier: CA2804915001
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152532_80152614del , CM000677.2:g.80152532_80152614del GRCh38
NC_000015.9:g.80444874_80444956del , CM000677.1:g.80444874_80444956del GRCh37
NC_000015.8:g.78231929_78232011del NCBI36
NG_012833.1:g.4534_4616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-43_-30+69del