Canonical Allele Identifier: CA971894296
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152781G>C , CM000677.2:g.80152781G>C GRCh38
NC_000015.9:g.80445123G>C , CM000677.1:g.80445123G>C GRCh37
NC_000015.8:g.78232178G>C NCBI36
NG_012833.1:g.4783G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000407106.5:c.-154G>C ENSP00000385080.1:n.-154G>C
ENST00000558022.5:c.-30+236G>C ENSP00000453152.1:n.-30+236G>C