Canonical Allele Identifier: CA2556700145
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152504-GCT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152506_80152507del , CM000677.2:g.80152506_80152507del GRCh38
NC_000015.9:g.80444848_80444849del , CM000677.1:g.80444848_80444849del GRCh37
NC_000015.8:g.78231903_78231904del NCBI36
NG_012833.1:g.4508_4509del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-69_-68del ENSP00000453152.1:n.-69_-68del
Search 100 bp 5'
Search 100 bp 3'