Canonical Allele Identifier: CA2629872806
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152800G>A , CM000677.2:g.80152800G>A GRCh38
NC_000015.9:g.80445142G>A , CM000677.1:g.80445142G>A GRCh37
NC_000015.8:g.78232197G>A NCBI36
NG_012833.1:g.4802G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558767.6:c.-255G>A ENSP00000507680.1:n.-255G>A
ENST00000261755.9:c.-71G>A ENSP00000261755.5:n.-71G>A
ENST00000407106.5:c.-135G>A ENSP00000385080.1:n.-135G>A
ENST00000537726.5:n.12G>A
ENST00000558022.5:c.-29-226G>A ENSP00000453152.1:n.-29-226G>A
ENST00000558767.5:n.7G>A
NM_001374377.1:c.-135G>A NP_001361306.1:n.-135G>A
NM_001374380.1:c.-71G>A NP_001361309.1:n.-71G>A