Canonical Allele Identifier: CA2274723116
Gene: LINC00469 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811529_73811531delinsCCT , CM000679.2:g.73811529_73811531delinsCCT GRCh38
NC_000017.10:g.71807668_71807670delinsCCT , CM000679.1:g.71807668_71807670delinsCCT GRCh37
NC_000017.9:g.69319263_69319265delinsCCT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12157_228+12159delinsAGG
Search 100 bp 5'
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