Canonical Allele Identifier: CA585120017
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1237647555

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531635T>C , CM000670.2:g.128531635T>C GRCh38
NC_000008.10:g.129543881T>C , CM000670.1:g.129543881T>C GRCh37
NC_000008.9:g.129613063T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29435A>G