Canonical Allele Identifier: CA951840642
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1185771360

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399089G>A , CM000674.2:g.111399089G>A GRCh38
NC_000012.11:g.111836893G>A , CM000674.1:g.111836893G>A GRCh37
NC_000012.10:g.110321276G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2216G>A