Canonical Allele Identifier: CA2159874864
Gene: LINC02323 HGNC NCBI

Linked Data

dbSNP Id: rs1892859075

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102573849C>T , CM000676.2:g.102573849C>T GRCh38
NC_000014.8:g.103040186C>T , CM000676.1:g.103040186C>T GRCh37
NC_000014.7:g.102109939C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944240.1:n.609-6238C>T