Canonical Allele Identifier: CA2718120613
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1279239875

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546837C>T , CM000670.2:g.128546837C>T GRCh38
NC_000008.10:g.129559083C>T , CM000670.1:g.129559083C>T GRCh37
NC_000008.9:g.129628265C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14233G>A