Canonical Allele Identifier: CA971893280
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1595888217
gnomAD v3: 15-80152538-A-C
gnomAD v4: 15-80152538-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152538A>C , CM000677.2:g.80152538A>C GRCh38
NC_000015.9:g.80444880A>C , CM000677.1:g.80444880A>C GRCh37
NC_000015.8:g.78231935A>C NCBI36
NG_012833.1:g.4540A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-37A>C ENSP00000453152.1:n.-37A>C
Search 100 bp 5'
Search 100 bp 3'