Canonical Allele Identifier: CA2629872776
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152787_80152806dup , CM000677.2:g.80152787_80152806dup GRCh38
NC_000015.9:g.80445129_80445148dup , CM000677.1:g.80445129_80445148dup GRCh37
NC_000015.8:g.78232184_78232203dup NCBI36
NG_012833.1:g.4789_4808dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000407106.5:c.-148_-129dup ENSP00000385080.1:n.-148_-129dup
ENST00000558022.5:c.-29-239_-29-220dup ENSP00000453152.1:n.-29-239_-29-220dup