Canonical Allele Identifier: CA2629872428
Gene: FAH HGNC NCBI

Linked Data

gnomAD v4: 15-80152502-G-GGATGGA
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152503_80152504insATGGAG , CM000677.2:g.80152503_80152504insATGGAG GRCh38
NC_000015.9:g.80444845_80444846insATGGAG , CM000677.1:g.80444845_80444846insATGGAG GRCh37
NC_000015.8:g.78231900_78231901insATGGAG NCBI36
NG_012833.1:g.4505_4506insATGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-72_-71insATGGAG ENSP00000453152.1:n.-72_-71insATGGAG
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