Canonical Allele Identifier: CA2137750530
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1893196058

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824260del , CM000676.2:g.53824260del GRCh38
NC_000014.8:g.54290978del , CM000676.1:g.54290978del GRCh37
NC_000014.7:g.53360728del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25462del
XR_943873.1:n.299+25555del
XR_943874.1:n.392+25462del
XR_943875.1:n.392+25462del
XR_943878.1:n.330-50244del
XR_001750967.2:n.416+25462del
XR_001750968.1:n.324+25555del
XR_943872.3:n.415+25462del
XR_943873.2:n.322+25555del
XR_943874.3:n.419+25462del