Canonical Allele Identifier: CA261458697
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs548929579

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824178C>A , CM000676.2:g.53824178C>A GRCh38
NC_000014.8:g.54290896C>A , CM000676.1:g.54290896C>A GRCh37
NC_000014.7:g.53360646C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25544G>T
XR_943873.1:n.299+25637G>T
XR_943874.1:n.392+25544G>T
XR_943875.1:n.392+25544G>T
XR_943878.1:n.330-50326C>A
XR_001750967.2:n.416+25544G>T
XR_001750968.1:n.324+25637G>T
XR_943872.3:n.415+25544G>T
XR_943873.2:n.322+25637G>T
XR_943874.3:n.419+25544G>T