Canonical Allele Identifier: CA1119097427
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816086633

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529789A>T , CM000670.2:g.128529789A>T GRCh38
NC_000008.10:g.129542035A>T , CM000670.1:g.129542035A>T GRCh37
NC_000008.9:g.129611217A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31281T>A