Canonical Allele Identifier: CA274415609

Gene: LINC02883

Linked Data

• dbSNP Id: rs894491530
• MyVariant Identifiers: chr15:g.86300163A>G (hg19) ; chr15:g.85756932A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756932A>G , CM000677.2:g.85756932A>G	GRCh38
NC_000015.9:g.86300163A>G , CM000677.1:g.86300163A>G	GRCh37
NC_000015.8:g.84101167A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+952T>C