Canonical Allele Identifier: CA274415664

Gene: LINC02883

Linked Data

• dbSNP Id: rs1022351028
• MyVariant Identifiers: chr15:g.86300259G>A (hg19) ; chr15:g.85757028G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85757028G>A , CM000677.2:g.85757028G>A	GRCh38
NC_000015.9:g.86300259G>A , CM000677.1:g.86300259G>A	GRCh37
NC_000015.8:g.84101263G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+856C>T