Canonical Allele Identifier: CA971893121
Gene: FAH HGNC NCBI

Linked Data

gnomAD v3: 15-80152505-CTCGGG-C
gnomAD v4: 15-80152505-CTCGGG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152506_80152510del , CM000677.2:g.80152506_80152510del GRCh38
NC_000015.9:g.80444848_80444852del , CM000677.1:g.80444848_80444852del GRCh37
NC_000015.8:g.78231903_78231907del NCBI36
NG_012833.1:g.4508_4512del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-69_-65del ENSP00000453152.1:n.-69_-65del
Search 100 bp 5'
Search 100 bp 3'