Canonical Allele Identifier: CA2629872772
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152779-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152779G>T , CM000677.2:g.80152779G>T GRCh38
NC_000015.9:g.80445121G>T , CM000677.1:g.80445121G>T GRCh37
NC_000015.8:g.78232176G>T NCBI36
NG_012833.1:g.4781G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+234G>T ENSP00000453152.1:n.-30+234G>T
Search 100 bp 5'
Search 100 bp 3'