Canonical Allele Identifier: CA972306103

Gene: LINC02883

Linked Data

• dbSNP Id: rs2089540261
• gnomAD v3: 15-85756945-C-A
• gnomAD v4: 15-85756945-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756945C>A , CM000677.2:g.85756945C>A	GRCh38
NC_000015.9:g.86300176C>A , CM000677.1:g.86300176C>A	GRCh37
NC_000015.8:g.84101180C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+939G>T