Canonical Allele Identifier: CA951840610
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1869951101

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398959T>G , CM000674.2:g.111398959T>G GRCh38
NC_000012.11:g.111836763T>G , CM000674.1:g.111836763T>G GRCh37
NC_000012.10:g.110321146T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2086T>G