Canonical Allele Identifier: CA5120373

Gene: ROR2

Linked Data

• ClinVar Variation Id: 289268
• ClinVar RCV Id: RCV000296968 ; RCV002518078
• dbSNP Id: rs775640546
• ExAC: 9:94486287 T / C
• gnomAD v2: 9-94486287-T-C
• gnomAD v3: 9-91724005-T-C
• gnomAD v4: 9-91724005-T-C
• MyVariant Identifiers: chr9:g.94486287T>C (hg19) ; chr9:g.91724005T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724005T>C , CM000671.2:g.91724005T>C	GRCh38
NC_000009.11:g.94486287T>C , CM000671.1:g.94486287T>C	GRCh37
NC_000009.10:g.93526108T>C	NCBI36
NG_008089.1:g.231158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2489A>G MANE Select	ENSP00000364860.3:p.Tyr830Cys
ENST00000375708.3:c.2489A>G	ENSP00000364860.3:p.Tyr830Cys
ENST00000375715.5:c.1920+149A>G	ENSP00000364867.1:n.1920+149A>G
ENST00000550066.5:n.2957A>G
NM_004560.3:c.2489A>G	NP_004551.2:p.Tyr830Cys
XM_005252008.3:c.2069A>G	XP_005252065.1:p.Tyr690Cys
XM_005252009.3:c.1286A>G	XP_005252066.1:p.Tyr429Cys
XM_006717121.2:c.2069A>G	XP_006717184.1:p.Tyr690Cys
XM_011518721.1:c.2069A>G	XP_011517023.1:p.Tyr690Cys
XM_005252008.4:c.2069A>G	XP_005252065.1:p.Tyr690Cys
XM_006717121.3:c.2069A>G	XP_006717184.1:p.Tyr690Cys
XM_017014762.1:c.2480A>G	XP_016870251.1:p.Tyr827Cys
XM_017014763.1:c.2069A>G	XP_016870252.1:p.Tyr690Cys
NM_004560.4:c.2489A>G MANE Select	NP_004551.2:p.Tyr830Cys