Canonical Allele Identifier: CA2190326644
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2041054958
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152526G>A , CM000677.2:g.80152526G>A GRCh38
NC_000015.9:g.80444868G>A , CM000677.1:g.80444868G>A GRCh37
NC_000015.8:g.78231923G>A NCBI36
NG_012833.1:g.4528G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-49G>A ENSP00000453152.1:n.-49G>A
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