Canonical Allele Identifier: CA972306048

Gene: LINC02883

Linked Data

• dbSNP Id: rs2089539711
• gnomAD v3: 15-85756817-C-T
• gnomAD v4: 15-85756817-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756817C>T , CM000677.2:g.85756817C>T	GRCh38
NC_000015.9:g.86300048C>T , CM000677.1:g.86300048C>T	GRCh37
NC_000015.8:g.84101052C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.420-861G>A