Canonical Allele Identifier: CA2731546220
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2151802222
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756959G>A , CM000677.2:g.85756959G>A GRCh38
NC_000015.9:g.86300190G>A , CM000677.1:g.86300190G>A GRCh37
NC_000015.8:g.84101194G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+925C>T
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