Canonical Allele Identifier: CA274415668

Gene: LINC02883

Linked Data

• dbSNP Id: rs1007032590
• MyVariant Identifiers: chr15:g.85757030C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85757030C>T , CM000677.2:g.85757030C>T	GRCh38
NC_000015.9:g.86300261C>T , CM000677.1:g.86300261C>T	GRCh37
NC_000015.8:g.84101265C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+854G>A