Canonical Allele Identifier: CA614254115
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1215582788

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824126_53824138del , CM000676.2:g.53824126_53824138del GRCh38
NC_000014.8:g.54290844_54290856del , CM000676.1:g.54290844_54290856del GRCh37
NC_000014.7:g.53360594_53360606del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25584_392+25596del
XR_943873.1:n.299+25677_299+25689del
XR_943874.1:n.392+25584_392+25596del
XR_943875.1:n.392+25584_392+25596del
XR_943878.1:n.330-50378_330-50366del
XR_001750967.2:n.416+25584_416+25596del
XR_001750968.1:n.324+25677_324+25689del
XR_943872.3:n.415+25584_415+25596del
XR_943873.2:n.322+25677_322+25689del
XR_943874.3:n.419+25584_419+25596del