Canonical Allele Identifier: CA683615277

Gene: LINC02356

Linked Data

• dbSNP Id: rs1360800604
• gnomAD v3: 12-111398956-G-A
• gnomAD v4: 12-111398956-G-A
• MyVariant Identifiers: chr12:g.111836760G>A (hg19) ; chr12:g.111398956G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398956G>A , CM000674.2:g.111398956G>A	GRCh38
NC_000012.11:g.111836760G>A , CM000674.1:g.111836760G>A	GRCh37
NC_000012.10:g.110321143G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2083G>A