Canonical Allele Identifier: CA607341387

Gene: LINC02356

Linked Data

• dbSNP Id: rs1373782775
• gnomAD v2: 12-111836679-G-A
• gnomAD v3: 12-111398875-G-A
• gnomAD v4: 12-111398875-G-A
• MyVariant Identifiers: chr12:g.111836679G>A (hg19) ; chr12:g.111398875G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398875G>A , CM000674.2:g.111398875G>A	GRCh38
NC_000012.11:g.111836679G>A , CM000674.1:g.111836679G>A	GRCh37
NC_000012.10:g.110321062G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2002G>A