Canonical Allele Identifier: CA619465436

Gene: LINC02883

Linked Data

• dbSNP Id: rs1237934123
• gnomAD v2: 15-86300250-AACT-A
• gnomAD v3: 15-85757019-AACT-A
• gnomAD v4: 15-85757019-AACT-A
• MyVariant Identifiers: chr15:g.86300251_86300253del (hg19) ; chr15:g.85757020_85757022del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85757020_85757022del , CM000677.2:g.85757020_85757022del	GRCh38
NC_000015.9:g.86300251_86300253del , CM000677.1:g.86300251_86300253del	GRCh37
NC_000015.8:g.84101255_84101257del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+862_419+864del