Canonical Allele Identifier: CA971893157
Gene: FAH HGNC NCBI

Linked Data

gnomAD v3: 15-80152511-G-GTTCGGGGGC
gnomAD v4: 15-80152511-G-GTTCGGGGGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152511_80152512insTTCGGGGGC , CM000677.2:g.80152511_80152512insTTCGGGGGC GRCh38
NC_000015.9:g.80444853_80444854insTTCGGGGGC , CM000677.1:g.80444853_80444854insTTCGGGGGC GRCh37
NC_000015.8:g.78231908_78231909insTTCGGGGGC NCBI36
NG_012833.1:g.4513_4514insTTCGGGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-64_-63insTTCGGGGGC ENSP00000453152.1:n.-64_-63insTTCGGGGGC
Search 100 bp 5'
Search 100 bp 3'