Canonical Allele Identifier: CA5120755

Gene: ROR2

Linked Data

• ClinVar Variation Id: 367509
• ClinVar RCV Id: RCV000263077 ; RCV000359431
• dbSNP Id: rs184670366
• ExAC: 9:94489035 A / G
• gnomAD v2: 9-94489035-A-G
• gnomAD v3: 9-91726753-A-G
• gnomAD v4: 9-91726753-A-G
• MyVariant Identifiers: chr9:g.94489035A>G (hg19) ; chr9:g.91726753A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726753A>G , CM000671.2:g.91726753A>G	GRCh38
NC_000009.11:g.94489035A>G , CM000671.1:g.94489035A>G	GRCh37
NC_000009.10:g.93528856A>G	NCBI36
NG_008089.1:g.228410T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1184-10T>C MANE Select	ENSP00000364860.3:n.1184-10T>C
ENST00000375708.3:c.1184-10T>C	ENSP00000364860.3:n.1184-10T>C
ENST00000375715.5:c.764-10T>C	ENSP00000364867.1:n.764-10T>C
ENST00000550066.5:n.1652-10T>C
NM_004560.3:c.1184-10T>C	NP_004551.2:n.1184-10T>C
XM_005252008.3:c.764-10T>C	XP_005252065.1:n.764-10T>C
XM_005252009.3:c.-20-10T>C	XP_005252066.1:n.-20-10T>C
XM_006717121.2:c.764-10T>C	XP_006717184.1:n.764-10T>C
XM_011518721.1:c.764-10T>C	XP_011517023.1:n.764-10T>C
NM_001318204.1:c.1150-10T>C	NP_001305133.1:n.1150-10T>C
XM_005252008.4:c.764-10T>C	XP_005252065.1:n.764-10T>C
XM_006717121.3:c.764-10T>C	XP_006717184.1:n.764-10T>C
XM_017014762.1:c.1175-10T>C	XP_016870251.1:n.1175-10T>C
XM_017014763.1:c.764-10T>C	XP_016870252.1:n.764-10T>C
XR_001746315.1:n.1393-10T>C
NM_004560.4:c.1184-10T>C MANE Select	NP_004551.2:n.1184-10T>C
NM_001318204.2:c.1150-10T>C	NP_001305133.1:n.1150-10T>C