Canonical Allele Identifier: CA2190327236
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2041060168

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152735A>G , CM000677.2:g.80152735A>G GRCh38
NC_000015.9:g.80445077A>G , CM000677.1:g.80445077A>G GRCh37
NC_000015.8:g.78232132A>G NCBI36
NG_012833.1:g.4737A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+190A>G ENSP00000453152.1:n.-30+190A>G