Canonical Allele Identifier: CA261458687
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs961942176

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824093del , CM000676.2:g.53824093del GRCh38
NC_000014.8:g.54290811del , CM000676.1:g.54290811del GRCh37
NC_000014.7:g.53360561del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25631del
XR_943873.1:n.299+25724del
XR_943874.1:n.392+25631del
XR_943875.1:n.392+25631del
XR_943878.1:n.330-50411del
XR_001750967.2:n.416+25631del
XR_001750968.1:n.324+25724del
XR_943872.3:n.415+25631del
XR_943873.2:n.322+25724del
XR_943874.3:n.419+25631del