Canonical Allele Identifier: CA1119101179
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs932772339

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547126dup , CM000670.2:g.128547126dup GRCh38
NC_000008.10:g.129559372dup , CM000670.1:g.129559372dup GRCh37
NC_000008.9:g.129628554dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13950dup