Canonical Allele Identifier: CA847304097
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs34606099
gnomAD v3: 8-128547095-C-CAAAAAA
gnomAD v4: 8-128547095-C-CAAAAAA
MyVariant Identifiers: chr8:g.129559341_129559342insAAAAAA (hg19) chr8:g.128547095_128547096insAAAAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547109_128547114dup , CM000670.2:g.128547109_128547114dup GRCh38
NC_000008.10:g.129559355_129559360dup , CM000670.1:g.129559355_129559360dup GRCh37
NC_000008.9:g.129628537_129628542dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13969_508+13974dup
Search 100 bp 5'
Search 100 bp 3'