Canonical Allele Identifier: CA274415542
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs559749211
MyVariant Identifiers: chr15:g.86300053G>A (hg19) chr15:g.85756822G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756822G>A , CM000677.2:g.85756822G>A GRCh38
NC_000015.9:g.86300053G>A , CM000677.1:g.86300053G>A GRCh37
NC_000015.8:g.84101057G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-866C>T
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