Canonical Allele Identifier: CA2274723168
Gene: LINC00469 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811630_73811631delinsCT , CM000679.2:g.73811630_73811631delinsCT GRCh38
NC_000017.10:g.71807769_71807770delinsCT , CM000679.1:g.71807769_71807770delinsCT GRCh37
NC_000017.9:g.69319364_69319365delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12057_228+12058delinsAG
Search 100 bp 5'
Search 100 bp 3'