Canonical Allele Identifier: CA971893276
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2142086011

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152536G>A , CM000677.2:g.80152536G>A GRCh38
NC_000015.9:g.80444878G>A , CM000677.1:g.80444878G>A GRCh37
NC_000015.8:g.78231933G>A NCBI36
NG_012833.1:g.4538G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-39G>A ENSP00000453152.1:n.-39G>A