Canonical Allele Identifier: CA868433517

Gene: ROR2

Linked Data

• ClinVar Variation Id: 2072417
• ClinVar RCV Id: RCV002962900
• dbSNP Id: rs1233466142
• gnomAD v4: 9-91726530-G-T
• MyVariant Identifiers: chr9:g.94488812G>T (hg19) ; chr9:g.91726530G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726530G>T , CM000671.2:g.91726530G>T	GRCh38
NC_000009.11:g.94488812G>T , CM000671.1:g.94488812G>T	GRCh37
NC_000009.10:g.93528633G>T	NCBI36
NG_008089.1:g.228633C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1386+11C>A MANE Select	ENSP00000364860.3:n.1386+11C>A
ENST00000375708.3:c.1386+11C>A	ENSP00000364860.3:n.1386+11C>A
ENST00000375715.5:c.966+11C>A	ENSP00000364867.1:n.966+11C>A
ENST00000550066.5:n.1854+11C>A
NM_004560.3:c.1386+11C>A	NP_004551.2:n.1386+11C>A
XM_005252008.3:c.966+11C>A	XP_005252065.1:n.966+11C>A
XM_005252009.3:c.183+11C>A	XP_005252066.1:n.183+11C>A
XM_006717121.2:c.966+11C>A	XP_006717184.1:n.966+11C>A
XM_011518721.1:c.966+11C>A	XP_011517023.1:n.966+11C>A
NM_001318204.1:c.*64C>A	NP_001305133.1:n.*64C>A
XM_005252008.4:c.966+11C>A	XP_005252065.1:n.966+11C>A
XM_006717121.3:c.966+11C>A	XP_006717184.1:n.966+11C>A
XM_017014762.1:c.1377+11C>A	XP_016870251.1:n.1377+11C>A
XM_017014763.1:c.966+11C>A	XP_016870252.1:n.966+11C>A
XR_001746315.1:n.1595+11C>A
NM_004560.4:c.1386+11C>A MANE Select	NP_004551.2:n.1386+11C>A
NM_001318204.2:c.*64C>A	NP_001305133.1:n.*64C>A