Canonical Allele Identifier: CA2190326631
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152523A= , CM000677.2:g.80152523A= GRCh38
NC_000015.9:g.80444865A= , CM000677.1:g.80444865A= GRCh37
NC_000015.8:g.78231920A= NCBI36
NG_012833.1:g.4525A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-52A= ENSP00000453152.1:n.-52A=