Canonical Allele Identifier: CA2629872759
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152772-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152772G>C , CM000677.2:g.80152772G>C GRCh38
NC_000015.9:g.80445114G>C , CM000677.1:g.80445114G>C GRCh37
NC_000015.8:g.78232169G>C NCBI36
NG_012833.1:g.4774G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+227G>C ENSP00000453152.1:n.-30+227G>C
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