Canonical Allele Identifier: CA2530546367
Gene: FAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152494G>A , CM000677.2:g.80152494G>A GRCh38
NC_000015.9:g.80444836G>A , CM000677.1:g.80444836G>A GRCh37
NC_000015.8:g.78231891G>A NCBI36
NG_012833.1:g.4496G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-81G>A ENSP00000453152.1:n.-81G>A
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Search 100 bp 3'