Canonical Allele Identifier: CA2718111412
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1033262620

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546955T>G , CM000670.2:g.128546955T>G GRCh38
NC_000008.10:g.129559201T>G , CM000670.1:g.129559201T>G GRCh37
NC_000008.9:g.129628383T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+14115A>C