Canonical Allele Identifier: CA683615260
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1348424067

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398898G>A , CM000674.2:g.111398898G>A GRCh38
NC_000012.11:g.111836702G>A , CM000674.1:g.111836702G>A GRCh37
NC_000012.10:g.110321085G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2025G>A