Canonical Allele Identifier: CA963278560
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1893197179

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824296A>C , CM000676.2:g.53824296A>C GRCh38
NC_000014.8:g.54291014A>C , CM000676.1:g.54291014A>C GRCh37
NC_000014.7:g.53360764A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943872.1:n.392+25426T>G
XR_943873.1:n.299+25519T>G
XR_943874.1:n.392+25426T>G
XR_943875.1:n.392+25426T>G
XR_943878.1:n.330-50208A>C
XR_001750967.2:n.416+25426T>G
XR_001750968.1:n.324+25519T>G
XR_943872.3:n.415+25426T>G
XR_943873.2:n.322+25519T>G
XR_943874.3:n.419+25426T>G