Canonical Allele Identifier: CA243588834

Gene: LINC02356

Linked Data

• dbSNP Id: rs887257947
• MyVariant Identifiers: chr12:g.111836655T>A (hg19) ; chr12:g.111398851T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398851T>A , CM000674.2:g.111398851T>A	GRCh38
NC_000012.11:g.111836655T>A , CM000674.1:g.111836655T>A	GRCh37
NC_000012.10:g.110321038T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+1978T>A