Canonical Allele Identifier: CA706884498
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1228460253

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824183G>A , CM000676.2:g.53824183G>A GRCh38
NC_000014.8:g.54290901G>A , CM000676.1:g.54290901G>A GRCh37
NC_000014.7:g.53360651G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25539C>T
XR_943873.1:n.299+25632C>T
XR_943874.1:n.392+25539C>T
XR_943875.1:n.392+25539C>T
XR_943878.1:n.330-50321G>A
XR_001750967.2:n.416+25539C>T
XR_001750968.1:n.324+25632C>T
XR_943872.3:n.415+25539C>T
XR_943873.2:n.322+25632C>T
XR_943874.3:n.419+25539C>T