Canonical Allele Identifier: CA2190326800
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152583A= , CM000677.2:g.80152583A= GRCh38
NC_000015.9:g.80444925A= , CM000677.1:g.80444925A= GRCh37
NC_000015.8:g.78231980A= NCBI36
NG_012833.1:g.4585A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+38A= ENSP00000453152.1:n.-30+38A=