Canonical Allele Identifier: CA261458700
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs144841691

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824198G>A , CM000676.2:g.53824198G>A GRCh38
NC_000014.8:g.54290916G>A , CM000676.1:g.54290916G>A GRCh37
NC_000014.7:g.53360666G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25524C>T
XR_943873.1:n.299+25617C>T
XR_943874.1:n.392+25524C>T
XR_943875.1:n.392+25524C>T
XR_943878.1:n.330-50306G>A
XR_001750967.2:n.416+25524C>T
XR_001750968.1:n.324+25617C>T
XR_943872.3:n.415+25524C>T
XR_943873.2:n.322+25617C>T
XR_943874.3:n.419+25524C>T