Canonical Allele Identifier: CA2580588747
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119117G>T , CM000665.2:g.157119117G>T GRCh38
NC_000003.11:g.156836906G>T , CM000665.1:g.156836906G>T GRCh37
NC_000003.10:g.158319600G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3759C>A