Canonical Allele Identifier: CA627574248
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs1397688284

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811495del , CM000679.2:g.73811495del GRCh38
NC_000017.10:g.71807634del , CM000679.1:g.71807634del GRCh37
NC_000017.9:g.69319229del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12194del