Canonical Allele Identifier: CA2063275098
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1869951966

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398987_111398996del , CM000674.2:g.111398987_111398996del GRCh38
NC_000012.11:g.111836791_111836800del , CM000674.1:g.111836791_111836800del GRCh37
NC_000012.10:g.110321174_110321183del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945342.1:n.44+2114_44+2123del