Canonical Allele Identifier: CA716533309
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs1346239867
MyVariant Identifiers: chr15:g.86300066_86300067insC (hg19) chr15:g.85756835_85756836insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756839dup , CM000677.2:g.85756839dup GRCh38
NC_000015.9:g.86300070dup , CM000677.1:g.86300070dup GRCh37
NC_000015.8:g.84101074dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-880dup
Search 100 bp 5'
Search 100 bp 3'