Canonical Allele Identifier: CA2190326938
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2041057163

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152621C>T , CM000677.2:g.80152621C>T GRCh38
NC_000015.9:g.80444963C>T , CM000677.1:g.80444963C>T GRCh37
NC_000015.8:g.78232018C>T NCBI36
NG_012833.1:g.4623C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+76C>T ENSP00000453152.1:n.-30+76C>T