Canonical Allele Identifier: CA971894312
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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