Canonical Allele Identifier: CA2274723169
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047488818

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811631del , CM000679.2:g.73811631del GRCh38
NC_000017.10:g.71807770del , CM000679.1:g.71807770del GRCh37
NC_000017.9:g.69319365del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12057del