Canonical Allele Identifier: CA11318192

Gene: LINC02580

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43098432A>G , CM000664.2:g.43098432A>G	GRCh38
NC_000002.11:g.43325570A>G , CM000664.1:g.43325570A>G	GRCh37
NC_000002.10:g.43179074A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_109976.1:n.412-392T>C
XR_940021.1:n.362-392T>C
XR_940022.1:n.198-392T>C
XR_940023.1:n.593-392T>C
XR_940024.1:n.860-392T>C
XR_940025.1:n.196-392T>C
XR_940026.1:n.488-392T>C
XR_940027.1:n.920-392T>C
XR_940028.1:n.922-392T>C
NR_151714.1:n.412-392T>C