Canonical Allele Identifier: CA373840903

Gene: ROR2

Linked Data

• ClinVar Variation Id: 594282
• ClinVar RCV Id: RCV000729540
• dbSNP Id: rs369545969
• MyVariant Identifiers: chr9:g.94519784G>C (hg19) ; chr9:g.91757502G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757502G>C , CM000671.2:g.91757502G>C	GRCh38
NC_000009.11:g.94519784G>C , CM000671.1:g.94519784G>C	GRCh37
NC_000009.10:g.93559605G>C	NCBI36
NG_008089.1:g.197661C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.233C>G MANE Select	ENSP00000364860.3:p.Thr78Arg
ENST00000375708.3:c.233C>G	ENSP00000364860.3:p.Thr78Arg
ENST00000375715.5:c.-188C>G	ENSP00000364867.1:n.-188C>G
ENST00000495386.5:n.496C>G
ENST00000546883.1:n.435C>G
ENST00000548585.2:n.99C>G
ENST00000550066.5:n.701C>G
NM_004560.3:c.233C>G	NP_004551.2:p.Thr78Arg
XM_005252008.3:c.-188C>G	XP_005252065.1:n.-188C>G
XM_006717121.2:c.-188C>G	XP_006717184.1:n.-188C>G
XM_011518721.1:c.-188C>G	XP_011517023.1:n.-188C>G
NM_001318204.1:c.233C>G	NP_001305133.1:p.Thr78Arg
XM_005252008.4:c.-188C>G	XP_005252065.1:n.-188C>G
XM_006717121.3:c.-188C>G	XP_006717184.1:n.-188C>G
XM_017014762.1:c.224C>G	XP_016870251.1:p.Thr75Arg
XM_017014763.1:c.-188C>G	XP_016870252.1:n.-188C>G
XR_001746315.1:n.476C>G
NM_004560.4:c.233C>G MANE Select	NP_004551.2:p.Thr78Arg
NM_001318204.2:c.233C>G	NP_001305133.1:p.Thr78Arg