Canonical Allele Identifier: CA2192801896
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2089539908
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756855C>A , CM000677.2:g.85756855C>A GRCh38
NC_000015.9:g.86300086C>A , CM000677.1:g.86300086C>A GRCh37
NC_000015.8:g.84101090C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-899G>T
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Search 100 bp 3'