Canonical Allele Identifier: CA2192802085
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs1209581572
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756968C>T , CM000677.2:g.85756968C>T GRCh38
NC_000015.9:g.86300199C>T , CM000677.1:g.86300199C>T GRCh37
NC_000015.8:g.84101203C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+916G>A
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Search 100 bp 3'