Canonical Allele Identifier: CA2190326863
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152602T= , CM000677.2:g.80152602T= GRCh38
NC_000015.9:g.80444944T= , CM000677.1:g.80444944T= GRCh37
NC_000015.8:g.78231999T= NCBI36
NG_012833.1:g.4604T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+57T= ENSP00000453152.1:n.-30+57T=