Canonical Allele Identifier: CA2629872526
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152609-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152609T>G , CM000677.2:g.80152609T>G GRCh38
NC_000015.9:g.80444951T>G , CM000677.1:g.80444951T>G GRCh37
NC_000015.8:g.78232006T>G NCBI36
NG_012833.1:g.4611T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+64T>G ENSP00000453152.1:n.-30+64T>G
Search 100 bp 5'
Search 100 bp 3'