Canonical Allele Identifier: CA1413661562
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1178092520

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119177G>A , CM000665.2:g.157119177G>A GRCh38
NC_000003.11:g.156836966G>A , CM000665.1:g.156836966G>A GRCh37
NC_000003.10:g.158319660G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3699C>T