Canonical Allele Identifier: CA1818908350
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816370677

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546774G>T , CM000670.2:g.128546774G>T GRCh38
NC_000008.10:g.129559020G>T , CM000670.1:g.129559020G>T GRCh37
NC_000008.9:g.129628202G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14296C>A