Canonical Allele Identifier: CA2190326558
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152500C= , CM000677.2:g.80152500C= GRCh38
NC_000015.9:g.80444842C= , CM000677.1:g.80444842C= GRCh37
NC_000015.8:g.78231897C= NCBI36
NG_012833.1:g.4502C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-75C= ENSP00000453152.1:n.-75C=