Canonical Allele Identifier: CA2190326942
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152623A= , CM000677.2:g.80152623A= GRCh38
NC_000015.9:g.80444965A= , CM000677.1:g.80444965A= GRCh37
NC_000015.8:g.78232020A= NCBI36
NG_012833.1:g.4625A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+78A= ENSP00000453152.1:n.-30+78A=