Canonical Allele Identifier: CA706884378
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1288076667

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824004A>T , CM000676.2:g.53824004A>T GRCh38
NC_000014.8:g.54290722A>T , CM000676.1:g.54290722A>T GRCh37
NC_000014.7:g.53360472A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25718T>A
XR_943873.1:n.299+25811T>A
XR_943874.1:n.392+25718T>A
XR_943875.1:n.392+25718T>A
XR_943878.1:n.330-50500A>T
XR_001750967.2:n.416+25718T>A
XR_001750968.1:n.324+25811T>A
XR_943872.3:n.415+25718T>A
XR_943873.2:n.322+25811T>A
XR_943874.3:n.419+25718T>A