Canonical Allele Identifier: CA2469672203
Gene: LINC00278 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3004542G= , CM000686.2:g.3004542G= GRCh38
NC_000024.9:g.2872583G= , CM000686.1:g.2872583G= GRCh37
NC_000024.8:g.2932583G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046502.1:n.222+1325G=