Canonical Allele Identifier: CA2063275027
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1869948775

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398883T>G , CM000674.2:g.111398883T>G GRCh38
NC_000012.11:g.111836687T>G , CM000674.1:g.111836687T>G GRCh37
NC_000012.10:g.110321070T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2010T>G