Canonical Allele Identifier: CA951840596
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1869949396

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398899G>A , CM000674.2:g.111398899G>A GRCh38
NC_000012.11:g.111836703G>A , CM000674.1:g.111836703G>A GRCh37
NC_000012.10:g.110321086G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2026G>A