Canonical Allele Identifier: CA2804915088
Gene: FAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152701T>A , CM000677.2:g.80152701T>A GRCh38
NC_000015.9:g.80445043T>A , CM000677.1:g.80445043T>A GRCh37
NC_000015.8:g.78232098T>A NCBI36
NG_012833.1:g.4703T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+156T>A ENSP00000453152.1:n.-30+156T>A
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