Canonical Allele Identifier: CA963278494

Gene: LINC02331

Linked Data

• dbSNP Id: rs1893193518
• gnomAD v3: 14-53824105-CCTT-C
• gnomAD v4: 14-53824105-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53824108_53824110del , CM000676.2:g.53824108_53824110del	GRCh38
NC_000014.8:g.54290826_54290828del , CM000676.1:g.54290826_54290828del	GRCh37
NC_000014.7:g.53360576_53360578del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943872.1:n.392+25614_392+25616del
XR_943873.1:n.299+25707_299+25709del
XR_943874.1:n.392+25614_392+25616del
XR_943875.1:n.392+25614_392+25616del
XR_943878.1:n.330-50396_330-50394del
XR_001750967.2:n.416+25614_416+25616del
XR_001750968.1:n.324+25707_324+25709del
XR_943872.3:n.415+25614_415+25616del
XR_943873.2:n.322+25707_322+25709del
XR_943874.3:n.419+25614_419+25616del