Canonical Allele Identifier: CA706884450
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1371980296
MyVariant Identifiers: chr14:g.54290841_54290843del (hg19) chr14:g.53824123_53824125del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824123_53824125del , CM000676.2:g.53824123_53824125del GRCh38
NC_000014.8:g.54290841_54290843del , CM000676.1:g.54290841_54290843del GRCh37
NC_000014.7:g.53360591_53360593del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25597_392+25599del
XR_943873.1:n.299+25690_299+25692del
XR_943874.1:n.392+25597_392+25599del
XR_943875.1:n.392+25597_392+25599del
XR_943878.1:n.330-50381_330-50379del
XR_001750967.2:n.416+25597_416+25599del
XR_001750968.1:n.324+25690_324+25692del
XR_943872.3:n.415+25597_415+25599del
XR_943873.2:n.322+25690_322+25692del
XR_943874.3:n.419+25597_419+25599del
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