Canonical Allele Identifier: CA619465432

Gene: LINC02883

Linked Data

• dbSNP Id: rs1284084921
• gnomAD v2: 15-86300155-A-G
• gnomAD v3: 15-85756924-A-G
• gnomAD v4: 15-85756924-A-G
• MyVariant Identifiers: chr15:g.86300155A>G (hg19) ; chr15:g.85756924A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756924A>G , CM000677.2:g.85756924A>G	GRCh38
NC_000015.9:g.86300155A>G , CM000677.1:g.86300155A>G	GRCh37
NC_000015.8:g.84101159A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+960T>C