Canonical Allele Identifier: CA2190326778
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152574C= , CM000677.2:g.80152574C= GRCh38
NC_000015.9:g.80444916C= , CM000677.1:g.80444916C= GRCh37
NC_000015.8:g.78231971C= NCBI36
NG_012833.1:g.4576C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+29C= ENSP00000453152.1:n.-30+29C=