Canonical Allele Identifier: CA2629872429
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152503-G-GAT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152503_80152504insAT , CM000677.2:g.80152503_80152504insAT GRCh38
NC_000015.9:g.80444845_80444846insAT , CM000677.1:g.80444845_80444846insAT GRCh37
NC_000015.8:g.78231900_78231901insAT NCBI36
NG_012833.1:g.4505_4506insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-72_-71insAT ENSP00000453152.1:n.-72_-71insAT
Search 100 bp 5'
Search 100 bp 3'