Canonical Allele Identifier: CA2190327084
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152658A= , CM000677.2:g.80152658A= GRCh38
NC_000015.9:g.80445000A= , CM000677.1:g.80445000A= GRCh37
NC_000015.8:g.78232055A= NCBI36
NG_012833.1:g.4660A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+113A= ENSP00000453152.1:n.-30+113A=