Canonical Allele Identifier: CA2274723105
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811517_73811520delinsCAAT , CM000679.2:g.73811517_73811520delinsCAAT GRCh38
NC_000017.10:g.71807656_71807659delinsCAAT , CM000679.1:g.71807656_71807659delinsCAAT GRCh37
NC_000017.9:g.69319251_69319254delinsCAAT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12168_228+12171delinsATTG