Canonical Allele Identifier: CA13368321

Gene: LINC02646

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.130258151T>C , CM000672.2:g.130258151T>C	GRCh38
NC_000010.10:g.132056415T>C , CM000672.1:g.132056415T>C	GRCh37
NC_000010.9:g.131946405T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011540452.1:c.174+44122T>C	XP_011538754.1:n.174+44122T>C
XM_011540453.1:c.333+6086T>C	XP_011538755.1:n.333+6086T>C
XR_946468.1:n.7228+44122T>C
XR_946469.1:n.7228+44122T>C
XR_946471.1:n.7228+44122T>C
XR_946472.1:n.7387+6086T>C
XR_946473.1:n.7228+44122T>C
XR_946474.1:n.7228+44122T>C
XR_946477.1:n.7228+44122T>C
XR_002957106.1:n.3104+44122T>C