Canonical Allele Identifier: CA971893619
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152621_80152622insTCTG , CM000677.2:g.80152621_80152622insTCTG GRCh38
NC_000015.9:g.80444963_80444964insTCTG , CM000677.1:g.80444963_80444964insTCTG GRCh37
NC_000015.8:g.78232018_78232019insTCTG NCBI36
NG_012833.1:g.4623_4624insTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+76_-30+77insTCTG ENSP00000453152.1:n.-30+76_-30+77insTCTG