Canonical Allele Identifier: CA1898447340
Gene: LINC02652 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.28463177T>A , CM000672.2:g.28463177T>A GRCh38
NC_000010.10:g.28752106T>A , CM000672.1:g.28752106T>A GRCh37
NC_000010.9:g.28792112T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_134496.1:n.94-26956A>T