Canonical Allele Identifier: CA2190327362
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152785C= , CM000677.2:g.80152785C= GRCh38
NC_000015.9:g.80445127C= , CM000677.1:g.80445127C= GRCh37
NC_000015.8:g.78232182C= NCBI36
NG_012833.1:g.4787C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407106.5:c.-150C= ENSP00000385080.1:n.-150C=
ENST00000558022.5:c.-29-241C= ENSP00000453152.1:n.-29-241C=