Canonical Allele Identifier: CA2190327213
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152722G= , CM000677.2:g.80152722G= GRCh38
NC_000015.9:g.80445064G= , CM000677.1:g.80445064G= GRCh37
NC_000015.8:g.78232119G= NCBI36
NG_012833.1:g.4724G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+177G= ENSP00000453152.1:n.-30+177G=