Canonical Allele Identifier: CA2190327445
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152821C= , CM000677.2:g.80152821C= GRCh38
NC_000015.9:g.80445163C= , CM000677.1:g.80445163C= GRCh37
NC_000015.8:g.78232218C= NCBI36
NG_012833.1:g.4823C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558767.6:c.-234C= ENSP00000507680.1:n.-234C=
ENST00000261755.9:c.-50C= ENSP00000261755.5:n.-50C=
ENST00000407106.5:c.-114C= ENSP00000385080.1:n.-114C=
ENST00000537726.5:n.33C=
ENST00000558022.5:c.-29-205C= ENSP00000453152.1:n.-29-205C=
ENST00000558767.5:n.28C=
NM_001374377.1:c.-114C= NP_001361306.1:n.-114C=
NM_001374380.1:c.-50C= NP_001361309.1:n.-50C=