Canonical Allele Identifier: CA2629872784
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152785-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152785C>A , CM000677.2:g.80152785C>A GRCh38
NC_000015.9:g.80445127C>A , CM000677.1:g.80445127C>A GRCh37
NC_000015.8:g.78232182C>A NCBI36
NG_012833.1:g.4787C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407106.5:c.-150C>A ENSP00000385080.1:n.-150C>A
ENST00000558022.5:c.-29-241C>A ENSP00000453152.1:n.-29-241C>A
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