Canonical Allele Identifier: CA2469673317
Gene: LINC00278 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3024109G= , CM000686.2:g.3024109G= GRCh38
NC_000024.9:g.2892150G= , CM000686.1:g.2892150G= GRCh37
NC_000024.8:g.2952150G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046502.1:n.222+20892G=