Canonical Allele Identifier: CA2159874844
Gene: LINC02323 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102573789C= , CM000676.2:g.102573789C= GRCh38
NC_000014.8:g.103040126C= , CM000676.1:g.103040126C= GRCh37
NC_000014.7:g.102109879C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944240.1:n.609-6298C=