Canonical Allele Identifier: CA1818922620
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816120732

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531719C>T , CM000670.2:g.128531719C>T GRCh38
NC_000008.10:g.129543965C>T , CM000670.1:g.129543965C>T GRCh37
NC_000008.9:g.129613147C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29351G>A