Canonical Allele Identifier: CA716533365

Gene: LINC02883

Linked Data

• dbSNP Id: rs1182376864
• gnomAD v3: 15-85756907-C-G
• gnomAD v4: 15-85756907-C-G
• MyVariant Identifiers: chr15:g.86300138C>G (hg19) ; chr15:g.85756907C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756907C>G , CM000677.2:g.85756907C>G	GRCh38
NC_000015.9:g.86300138C>G , CM000677.1:g.86300138C>G	GRCh37
NC_000015.8:g.84101142C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.420-951G>C