Canonical Allele Identifier: CA2274723072
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs79546944

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811460C>A , CM000679.2:g.73811460C>A GRCh38
NC_000017.10:g.71807599C>A , CM000679.1:g.71807599C>A GRCh37
NC_000017.9:g.69319194C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12228G>T