Canonical Allele Identifier: CA2274723066
Gene: LINC00469 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811442_73811446delinsTAAAC , CM000679.2:g.73811442_73811446delinsTAAAC GRCh38
NC_000017.10:g.71807581_71807585delinsTAAAC , CM000679.1:g.71807581_71807585delinsTAAAC GRCh37
NC_000017.9:g.69319176_69319180delinsTAAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12242_228+12246delinsGTTTA
Search 100 bp 5'
Search 100 bp 3'