Canonical Allele Identifier: CA274415597

Gene: LINC02883

Linked Data

• dbSNP Id: rs930640892
• MyVariant Identifiers: chr15:g.86300139T>C (hg19) ; chr15:g.85756908T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756908T>C , CM000677.2:g.85756908T>C	GRCh38
NC_000015.9:g.86300139T>C , CM000677.1:g.86300139T>C	GRCh37
NC_000015.8:g.84101143T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.420-952A>G