Canonical Allele Identifier: CA274415593

Gene: LINC02883

Linked Data

• dbSNP Id: rs897764742
• gnomAD v2: 15-86300136-C-T
• gnomAD v3: 15-85756905-C-T
• gnomAD v4: 15-85756905-C-T
• MyVariant Identifiers: chr15:g.86300136C>T (hg19) ; chr15:g.85756905C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756905C>T , CM000677.2:g.85756905C>T	GRCh38
NC_000015.9:g.86300136C>T , CM000677.1:g.86300136C>T	GRCh37
NC_000015.8:g.84101140C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.420-949G>A