Canonical Allele Identifier: CA2274723157
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047488685

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811613del , CM000679.2:g.73811613del GRCh38
NC_000017.10:g.71807752del , CM000679.1:g.71807752del GRCh37
NC_000017.9:g.69319347del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12080del