Canonical Allele Identifier: CA683615250

Gene: LINC02356

Linked Data

• dbSNP Id: rs1469105718
• MyVariant Identifiers: chr12:g.111836695del (hg19) ; chr12:g.111398891del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398892del , CM000674.2:g.111398892del	GRCh38
NC_000012.11:g.111836696del , CM000674.1:g.111836696del	GRCh37
NC_000012.10:g.110321079del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2019del