Canonical Allele Identifier: CA1055324271
Gene: LINC00880 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119175A>G , CM000665.2:g.157119175A>G GRCh38
NC_000003.11:g.156836964A>G , CM000665.1:g.156836964A>G GRCh37
NC_000003.10:g.158319658A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3701T>C