Canonical Allele Identifier: CA1413661547
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119160T= , CM000665.2:g.157119160T= GRCh38
NC_000003.11:g.156836949T= , CM000665.1:g.156836949T= GRCh37
NC_000003.10:g.158319643T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3716A=