Canonical Allele Identifier: CA2759045339
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119118G>A , CM000665.2:g.157119118G>A GRCh38
NC_000003.11:g.156836907G>A , CM000665.1:g.156836907G>A GRCh37
NC_000003.10:g.158319601G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3758C>T