Canonical Allele Identifier: CA971893259
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1595888206
gnomAD v3: 15-80152528-A-T
gnomAD v4: 15-80152528-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152528A>T , CM000677.2:g.80152528A>T GRCh38
NC_000015.9:g.80444870A>T , CM000677.1:g.80444870A>T GRCh37
NC_000015.8:g.78231925A>T NCBI36
NG_012833.1:g.4530A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-47A>T ENSP00000453152.1:n.-47A>T
Search 100 bp 5'
Search 100 bp 3'