Canonical Allele Identifier: CA619465435

Gene: LINC02883

Linked Data

• dbSNP Id: rs1186615019
• gnomAD v2: 15-86300242-C-T
• gnomAD v3: 15-85757011-C-T
• gnomAD v4: 15-85757011-C-T
• MyVariant Identifiers: chr15:g.86300242C>T (hg19) ; chr15:g.85757011C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85757011C>T , CM000677.2:g.85757011C>T	GRCh38
NC_000015.9:g.86300242C>T , CM000677.1:g.86300242C>T	GRCh37
NC_000015.8:g.84101246C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+873G>A