Canonical Allele Identifier: CA1119100981
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs34606099

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547114_128547115insAAAGAAAAAAAAAAATTATTTGAAAAAAAAAAAAAAAAAAAA , CM000670.2:g.128547114_128547115insAAAGAAAAAAAAAAATTATTTGAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000008.10:g.129559360_129559361insAAAGAAAAAAAAAAATTATTTGAAAAAAAAAAAAAAAAAAAA , CM000670.1:g.129559360_129559361insAAAGAAAAAAAAAAATTATTTGAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000008.9:g.129628542_129628543insAAAGAAAAAAAAAAATTATTTGAAAAAAAAAAAAAAAAAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13974_508+13975insTCAAATAATTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT