Canonical Allele Identifier: CA591597521

Gene: LINC02669

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3496602A>T , CM000672.2:g.3496602A>T	GRCh38
NC_000010.10:g.3538794A>T , CM000672.1:g.3538794A>T	GRCh37
NC_000010.9:g.3528794A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_131187.1:n.162+177746A>T
XR_930569.1:n.541+1051T>A
XR_930570.1:n.542-4T>A
XR_930571.1:n.541+1051T>A
XR_930572.1:n.562+1051T>A
XR_930573.1:n.541+1051T>A
XR_930574.1:n.541+1051T>A
NR_155743.1:n.631+1051T>A
NR_155744.1:n.632-4T>A
NR_155745.1:n.632-4T>A
NR_155746.1:n.632-366T>A
XR_001747322.1:n.2230+1051T>A
XR_001747323.1:n.2091+1051T>A
XR_001747324.1:n.2230+1051T>A
XR_001747326.1:n.2071+1051T>A
XR_001747327.1:n.2230+1051T>A
XR_002957056.1:n.1961+1051T>A
XR_002957057.1:n.2119-4T>A
XR_002957058.1:n.1961+1051T>A
XR_930569.2:n.1955+1051T>A