Canonical Allele Identifier: CA243589002

Gene: LINC02356

Linked Data

• dbSNP Id: rs979413064
• gnomAD v3: 12-111399001-A-T
• gnomAD v4: 12-111399001-A-T
• MyVariant Identifiers: chr12:g.111836805A>T (hg19) ; chr12:g.111399001A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111399001A>T , CM000674.2:g.111399001A>T	GRCh38
NC_000012.11:g.111836805A>T , CM000674.1:g.111836805A>T	GRCh37
NC_000012.10:g.110321188A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2128A>T