Canonical Allele Identifier: CA2274723100
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs1661913328

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811508dup , CM000679.2:g.73811508dup GRCh38
NC_000017.10:g.71807647dup , CM000679.1:g.71807647dup GRCh37
NC_000017.9:g.69319242dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12180dup