Canonical Allele Identifier: CA2190327282
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1595888378

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152760C>T , CM000677.2:g.80152760C>T GRCh38
NC_000015.9:g.80445102C>T , CM000677.1:g.80445102C>T GRCh37
NC_000015.8:g.78232157C>T NCBI36
NG_012833.1:g.4762C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+215C>T ENSP00000453152.1:n.-30+215C>T