Canonical Allele Identifier: CA963278508
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1893194324

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824131A>G , CM000676.2:g.53824131A>G GRCh38
NC_000014.8:g.54290849A>G , CM000676.1:g.54290849A>G GRCh37
NC_000014.7:g.53360599A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25591T>C
XR_943873.1:n.299+25684T>C
XR_943874.1:n.392+25591T>C
XR_943875.1:n.392+25591T>C
XR_943878.1:n.330-50373A>G
XR_001750967.2:n.416+25591T>C
XR_001750968.1:n.324+25684T>C
XR_943872.3:n.415+25591T>C
XR_943873.2:n.322+25684T>C
XR_943874.3:n.419+25591T>C