Canonical Allele Identifier: CA619465440

Gene: LINC02883

Linked Data

• dbSNP Id: rs1160847567
• gnomAD v2: 15-86300268-G-C
• gnomAD v3: 15-85757037-G-C
• gnomAD v4: 15-85757037-G-C
• MyVariant Identifiers: chr15:g.86300268G>C (hg19) ; chr15:g.85757037G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85757037G>C , CM000677.2:g.85757037G>C	GRCh38
NC_000015.9:g.86300268G>C , CM000677.1:g.86300268G>C	GRCh37
NC_000015.8:g.84101272G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+847C>G