Canonical Allele Identifier: CA1119100826
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1413663593

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546967T>G , CM000670.2:g.128546967T>G GRCh38
NC_000008.10:g.129559213T>G , CM000670.1:g.129559213T>G GRCh37
NC_000008.9:g.129628395T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14103A>C