Canonical Allele Identifier: CA2192802057
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2089540324
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756958G>C , CM000677.2:g.85756958G>C GRCh38
NC_000015.9:g.86300189G>C , CM000677.1:g.86300189G>C GRCh37
NC_000015.8:g.84101193G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+926C>G
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