Canonical Allele Identifier: CA2629872780
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152784-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152784G>A , CM000677.2:g.80152784G>A GRCh38
NC_000015.9:g.80445126G>A , CM000677.1:g.80445126G>A GRCh37
NC_000015.8:g.78232181G>A NCBI36
NG_012833.1:g.4786G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407106.5:c.-151G>A ENSP00000385080.1:n.-151G>A
ENST00000558022.5:c.-30+239G>A ENSP00000453152.1:n.-30+239G>A
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