Canonical Allele Identifier: CA2137750412
Gene: LINC02331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824000G= , CM000676.2:g.53824000G= GRCh38
NC_000014.8:g.54290718G= , CM000676.1:g.54290718G= GRCh37
NC_000014.7:g.53360468G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25722C=
XR_943873.1:n.299+25815C=
XR_943874.1:n.392+25722C=
XR_943875.1:n.392+25722C=
XR_943878.1:n.330-50504G=
XR_001750967.2:n.416+25722C=
XR_001750968.1:n.324+25815C=
XR_943872.3:n.415+25722C=
XR_943873.2:n.322+25815C=
XR_943874.3:n.419+25722C=