Canonical Allele Identifier: CA683615325

Gene: LINC02356

Linked Data

• dbSNP Id: rs1171817351
• gnomAD v3: 12-111399067-A-G
• gnomAD v4: 12-111399067-A-G
• MyVariant Identifiers: chr12:g.111836871A>G (hg19) ; chr12:g.111399067A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111399067A>G , CM000674.2:g.111399067A>G	GRCh38
NC_000012.11:g.111836871A>G , CM000674.1:g.111836871A>G	GRCh37
NC_000012.10:g.110321254A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2194A>G