Canonical Allele Identifier: CA2190326561
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152501G= , CM000677.2:g.80152501G= GRCh38
NC_000015.9:g.80444843G= , CM000677.1:g.80444843G= GRCh37
NC_000015.8:g.78231898G= NCBI36
NG_012833.1:g.4503G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-74G= ENSP00000453152.1:n.-74G=