Canonical Allele Identifier: CA1413661546
Gene: LINC00880 HGNC NCBI

Linked Data

dbSNP Id: rs1737282970

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119158T>C , CM000665.2:g.157119158T>C GRCh38
NC_000003.11:g.156836947T>C , CM000665.1:g.156836947T>C GRCh37
NC_000003.10:g.158319641T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3718A>G