Canonical Allele Identifier: CA971893234
Gene: FAH HGNC NCBI

Linked Data

gnomAD v3: 15-80152519-C-G
gnomAD v4: 15-80152519-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152519C>G , CM000677.2:g.80152519C>G GRCh38
NC_000015.9:g.80444861C>G , CM000677.1:g.80444861C>G GRCh37
NC_000015.8:g.78231916C>G NCBI36
NG_012833.1:g.4521C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-56C>G ENSP00000453152.1:n.-56C>G
Search 100 bp 5'
Search 100 bp 3'