Canonical Allele Identifier: CA2629872540
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152615-G-GGGT
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152615_80152616insGGT , CM000677.2:g.80152615_80152616insGGT GRCh38
NC_000015.9:g.80444957_80444958insGGT , CM000677.1:g.80444957_80444958insGGT GRCh37
NC_000015.8:g.78232012_78232013insGGT NCBI36
NG_012833.1:g.4617_4618insGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+70_-30+71insGGT ENSP00000453152.1:n.-30+70_-30+71insGGT
Search 100 bp 5'
Search 100 bp 3'