Canonical Allele Identifier: CA1480021911
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99474213_99474216delinsTAGG , CM000666.2:g.99474213_99474216delinsTAGG GRCh38
NC_000004.11:g.100395370_100395373delinsTAGG , CM000666.1:g.100395370_100395373delinsTAGG GRCh37
NC_000004.10:g.100614393_100614396delinsTAGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506494.1:n.243-2354_243-2351delinsCCTA
Search 100 bp 5'
Search 100 bp 3'