Canonical Allele Identifier: CA847294999
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1364325312

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531652G>A , CM000670.2:g.128531652G>A GRCh38
NC_000008.10:g.129543898G>A , CM000670.1:g.129543898G>A GRCh37
NC_000008.9:g.129613080G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29418C>T