Canonical Allele Identifier: CA2137750548
Gene: LINC02331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824292C= , CM000676.2:g.53824292C= GRCh38
NC_000014.8:g.54291010C= , CM000676.1:g.54291010C= GRCh37
NC_000014.7:g.53360760C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25430G=
XR_943873.1:n.299+25523G=
XR_943874.1:n.392+25430G=
XR_943875.1:n.392+25430G=
XR_943878.1:n.330-50212C=
XR_001750967.2:n.416+25430G=
XR_001750968.1:n.324+25523G=
XR_943872.3:n.415+25430G=
XR_943873.2:n.322+25523G=
XR_943874.3:n.419+25430G=