Canonical Allele Identifier: CA656100756
Gene: LINC02331 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53823851C>G , CM000676.2:g.53823851C>G GRCh38
NC_000014.8:g.54290569C>G , CM000676.1:g.54290569C>G GRCh37
NC_000014.7:g.53360319C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25871G>C
XR_943873.1:n.299+25964G>C
XR_943874.1:n.392+25871G>C
XR_943875.1:n.392+25871G>C
XR_943878.1:n.330-50653C>G
XR_001750967.2:n.416+25871G>C
XR_001750968.1:n.324+25964G>C
XR_943872.3:n.415+25871G>C
XR_943873.2:n.322+25964G>C
XR_943874.3:n.419+25871G>C