Canonical Allele Identifier: CA2804915059
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152655C>T , CM000677.2:g.80152655C>T GRCh38
NC_000015.9:g.80444997C>T , CM000677.1:g.80444997C>T GRCh37
NC_000015.8:g.78232052C>T NCBI36
NG_012833.1:g.4657C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+110C>T ENSP00000453152.1:n.-30+110C>T