Canonical Allele Identifier: CA1863921732

Gene: ROR2

Linked Data

• ClinVar Variation Id: 997999
• ClinVar RCV Id: RCV001310271 ; RCV001293680
• dbSNP Id: rs1836888405

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723870dup , CM000671.2:g.91723870dup	GRCh38
NC_000009.11:g.94486152dup , CM000671.1:g.94486152dup	GRCh37
NC_000009.10:g.93525973dup	NCBI36
NG_008089.1:g.231294dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2625dup MANE Select	ENSP00000364860.3:p.Thr876HisfsTer20
ENST00000375708.3:c.2625dup	ENSP00000364860.3:p.Thr876HisfsTer20
ENST00000375715.5:c.1920+285dup	ENSP00000364867.1:n.1920+285dup
ENST00000550066.5:n.3093dup
NM_004560.3:c.2625dup	NP_004551.2:p.Thr876HisfsTer20
XM_005252008.3:c.2205dup	XP_005252065.1:p.Thr736HisfsTer20
XM_005252009.3:c.1422dup	XP_005252066.1:p.Thr475HisfsTer20
XM_006717121.2:c.2205dup	XP_006717184.1:p.Thr736HisfsTer20
XM_011518721.1:c.2205dup	XP_011517023.1:p.Thr736HisfsTer20
XM_005252008.4:c.2205dup	XP_005252065.1:p.Thr736HisfsTer20
XM_006717121.3:c.2205dup	XP_006717184.1:p.Thr736HisfsTer20
XM_017014762.1:c.2616dup	XP_016870251.1:p.Thr873HisfsTer20
XM_017014763.1:c.2205dup	XP_016870252.1:p.Thr736HisfsTer20
NM_004560.4:c.2625dup MANE Select	NP_004551.2:p.Thr876HisfsTer20