Canonical Allele Identifier: CA1898447339
Community Standard Title: NC_000010.11:g.28463177T=
Gene: LINC02652 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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