Canonical Allele Identifier: CA614254082
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1186180221

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53823996del , CM000676.2:g.53823996del GRCh38
NC_000014.8:g.54290714del , CM000676.1:g.54290714del GRCh37
NC_000014.7:g.53360464del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25727del
XR_943873.1:n.299+25820del
XR_943874.1:n.392+25727del
XR_943875.1:n.392+25727del
XR_943878.1:n.330-50508del
XR_001750967.2:n.416+25727del
XR_001750968.1:n.324+25820del
XR_943872.3:n.415+25727del
XR_943873.2:n.322+25820del
XR_943874.3:n.419+25727del