Canonical Allele Identifier: CA2137750439
Gene: LINC02331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824062T= , CM000676.2:g.53824062T= GRCh38
NC_000014.8:g.54290780T= , CM000676.1:g.54290780T= GRCh37
NC_000014.7:g.53360530T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25660A=
XR_943873.1:n.299+25753A=
XR_943874.1:n.392+25660A=
XR_943875.1:n.392+25660A=
XR_943878.1:n.330-50442T=
XR_001750967.2:n.416+25660A=
XR_001750968.1:n.324+25753A=
XR_943872.3:n.415+25660A=
XR_943873.2:n.322+25753A=
XR_943874.3:n.419+25660A=