Canonical Allele Identifier: CA1119100816
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816372408

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546879del , CM000670.2:g.128546879del GRCh38
NC_000008.10:g.129559125del , CM000670.1:g.129559125del GRCh37
NC_000008.9:g.129628307del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14191del