Canonical Allele Identifier: CA1413661716
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119320T= , CM000665.2:g.157119320T= GRCh38
NC_000003.11:g.156837109T= , CM000665.1:g.156837109T= GRCh37
NC_000003.10:g.158319803T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3556A=