Canonical Allele Identifier: CA607341392

Gene: LINC02356

Linked Data

• dbSNP Id: rs149212747
• gnomAD v2: 12-111836771-AC-A
• gnomAD v3: 12-111398967-AC-A
• gnomAD v4: 12-111398967-AC-A
• MyVariant Identifiers: chr12:g.111836772del (hg19) ; chr12:g.111398968del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398974del , CM000674.2:g.111398974del	GRCh38
NC_000012.11:g.111836778del , CM000674.1:g.111836778del	GRCh37
NC_000012.10:g.110321161del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_945342.1:n.44+2101del