Canonical Allele Identifier: CA2190327364
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152786G= , CM000677.2:g.80152786G= GRCh38
NC_000015.9:g.80445128G= , CM000677.1:g.80445128G= GRCh37
NC_000015.8:g.78232183G= NCBI36
NG_012833.1:g.4788G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407106.5:c.-149G= ENSP00000385080.1:n.-149G=
ENST00000558022.5:c.-29-240G= ENSP00000453152.1:n.-29-240G=