Canonical Allele Identifier: CA2190327379
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152792C= , CM000677.2:g.80152792C= GRCh38
NC_000015.9:g.80445134C= , CM000677.1:g.80445134C= GRCh37
NC_000015.8:g.78232189C= NCBI36
NG_012833.1:g.4794C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407106.5:c.-143C= ENSP00000385080.1:n.-143C=
ENST00000537726.5:n.4C=
ENST00000558022.5:c.-29-234C= ENSP00000453152.1:n.-29-234C=
NM_001374377.1:c.-143C= NP_001361306.1:n.-143C=
NM_001374380.1:c.-79C= NP_001361309.1:n.-79C=