Canonical Allele Identifier: CA2137750472
Gene: LINC02331 HGNC NCBI

Linked Data

dbSNP Id: rs1893193934

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53824121G>C , CM000676.2:g.53824121G>C GRCh38
NC_000014.8:g.54290839G>C , CM000676.1:g.54290839G>C GRCh37
NC_000014.7:g.53360589G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943872.1:n.392+25601C>G
XR_943873.1:n.299+25694C>G
XR_943874.1:n.392+25601C>G
XR_943875.1:n.392+25601C>G
XR_943878.1:n.330-50383G>C
XR_001750967.2:n.416+25601C>G
XR_001750968.1:n.324+25694C>G
XR_943872.3:n.415+25601C>G
XR_943873.2:n.322+25694C>G
XR_943874.3:n.419+25601C>G