Canonical Allele Identifier: CA2469674509
Gene: LINC00278 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3042992G= , CM000686.2:g.3042992G= GRCh38
NC_000024.9:g.2911033G= , CM000686.1:g.2911033G= GRCh37
NC_000024.8:g.2971033G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046502.1:n.223-36292G=