Canonical Allele Identifier: CA963278450
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1893192277

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824039T>C , CM000676.2:g.53824039T>C GRCh38
NC_000014.8:g.54290757T>C , CM000676.1:g.54290757T>C GRCh37
NC_000014.7:g.53360507T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25683A>G
XR_943873.1:n.299+25776A>G
XR_943874.1:n.392+25683A>G
XR_943875.1:n.392+25683A>G
XR_943878.1:n.330-50465T>C
XR_001750967.2:n.416+25683A>G
XR_001750968.1:n.324+25776A>G
XR_943872.3:n.415+25683A>G
XR_943873.2:n.322+25776A>G
XR_943874.3:n.419+25683A>G