Canonical Allele Identifier: CA2190326981
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152636G= , CM000677.2:g.80152636G= GRCh38
NC_000015.9:g.80444978G= , CM000677.1:g.80444978G= GRCh37
NC_000015.8:g.78232033G= NCBI36
NG_012833.1:g.4638G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+91G= ENSP00000453152.1:n.-30+91G=