Canonical Allele Identifier: CA716533386

Gene: LINC02883

Linked Data

• dbSNP Id: rs1314481374
• gnomAD v3: 15-85756961-G-A
• gnomAD v4: 15-85756961-G-A
• MyVariant Identifiers: chr15:g.86300192G>A (hg19) ; chr15:g.85756961G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756961G>A , CM000677.2:g.85756961G>A	GRCh38
NC_000015.9:g.86300192G>A , CM000677.1:g.86300192G>A	GRCh37
NC_000015.8:g.84101196G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+923C>T