Canonical Allele Identifier: CA1119100833
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816376062

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547050C>A , CM000670.2:g.128547050C>A GRCh38
NC_000008.10:g.129559296C>A , CM000670.1:g.129559296C>A GRCh37
NC_000008.9:g.129628478C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14020G>T