Canonical Allele Identifier: CA1818909534
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816379468

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547154G>A , CM000670.2:g.128547154G>A GRCh38
NC_000008.10:g.129559400G>A , CM000670.1:g.129559400G>A GRCh37
NC_000008.9:g.129628582G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13916C>T