Canonical Allele Identifier: CA1119100821
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816372888

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546929del , CM000670.2:g.128546929del GRCh38
NC_000008.10:g.129559175del , CM000670.1:g.129559175del GRCh37
NC_000008.9:g.129628357del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+14142del