Canonical Allele Identifier: CA1413661597
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119221A= , CM000665.2:g.157119221A= GRCh38
NC_000003.11:g.156837010A= , CM000665.1:g.156837010A= GRCh37
NC_000003.10:g.158319704A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3655T=