Canonical Allele Identifier: CA683615339

Gene: LINC02356

Linked Data

• dbSNP Id: rs1211454158
• MyVariant Identifiers: chr12:g.111836904T>C (hg19) ; chr12:g.111399100T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111399100T>C , CM000674.2:g.111399100T>C	GRCh38
NC_000012.11:g.111836904T>C , CM000674.1:g.111836904T>C	GRCh37
NC_000012.10:g.110321287T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2227T>C