Canonical Allele Identifier: CA173318

Gene: ROR2

Linked Data

• ClinVar Variation Id: 159813
• ClinVar RCV Id: RCV000147384 ; RCV000171424 ; RCV001353137
• dbSNP Id: rs529829552
• ExAC: 9:94486806 C / T
• gnomAD v2: 9-94486806-C-T
• gnomAD v3: 9-91724524-C-T
• gnomAD v4: 9-91724524-C-T
• MyVariant Identifiers: chr9:g.94486806C>T (hg19) ; chr9:g.91724524C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724524C>T , CM000671.2:g.91724524C>T	GRCh38
NC_000009.11:g.94486806C>T , CM000671.1:g.94486806C>T	GRCh37
NC_000009.10:g.93526627C>T	NCBI36
NG_008089.1:g.230639G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1970G>A MANE Select	ENSP00000364860.3:p.Arg657His
ENST00000375708.3:c.1970G>A	ENSP00000364860.3:p.Arg657His
ENST00000375715.5:c.1550G>A	ENSP00000364867.1:p.Arg517His
ENST00000550066.5:n.2438G>A
NM_004560.3:c.1970G>A	NP_004551.2:p.Arg657His
XM_005252008.3:c.1550G>A	XP_005252065.1:p.Arg517His
XM_005252009.3:c.767G>A	XP_005252066.1:p.Arg256His
XM_006717121.2:c.1550G>A	XP_006717184.1:p.Arg517His
XM_011518721.1:c.1550G>A	XP_011517023.1:p.Arg517His
XM_005252008.4:c.1550G>A	XP_005252065.1:p.Arg517His
XM_006717121.3:c.1550G>A	XP_006717184.1:p.Arg517His
XM_017014762.1:c.1961G>A	XP_016870251.1:p.Arg654His
XM_017014763.1:c.1550G>A	XP_016870252.1:p.Arg517His
NM_004560.4:c.1970G>A MANE Select	NP_004551.2:p.Arg657His