Canonical Allele Identifier: CA868452844

Gene: ROR2

Linked Data

• dbSNP Id: rs1301817892
• gnomAD v3: 9-91757566-AGG-A
• gnomAD v4: 9-91757566-AGG-A
• MyVariant Identifiers: chr9:g.94519849_94519850del (hg19) ; chr9:g.91757567_91757568del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757567_91757568del , CM000671.2:g.91757567_91757568del	GRCh38
NC_000009.11:g.94519849_94519850del , CM000671.1:g.94519849_94519850del	GRCh37
NC_000009.10:g.93559670_93559671del	NCBI36
NG_008089.1:g.197595_197596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.176-9_176-8del MANE Select	ENSP00000364860.3:n.176-9_176-8del
ENST00000375708.3:c.176-9_176-8del	ENSP00000364860.3:n.176-9_176-8del
ENST00000375715.5:c.-245-9_-245-8del	ENSP00000364867.1:n.-245-9_-245-8del
ENST00000495386.5:n.439-9_439-8del
ENST00000546883.1:n.378-9_378-8del
ENST00000548585.2:n.42-9_42-8del
ENST00000550066.5:n.644-9_644-8del
NM_004560.3:c.176-9_176-8del	NP_004551.2:n.176-9_176-8del
XM_005252008.3:c.-245-9_-245-8del	XP_005252065.1:n.-245-9_-245-8del
XM_006717121.2:c.-245-9_-245-8del	XP_006717184.1:n.-245-9_-245-8del
XM_011518721.1:c.-245-9_-245-8del	XP_011517023.1:n.-245-9_-245-8del
NM_001318204.1:c.176-9_176-8del	NP_001305133.1:n.176-9_176-8del
XM_005252008.4:c.-245-9_-245-8del	XP_005252065.1:n.-245-9_-245-8del
XM_006717121.3:c.-245-9_-245-8del	XP_006717184.1:n.-245-9_-245-8del
XM_017014762.1:c.167-9_167-8del	XP_016870251.1:n.167-9_167-8del
XM_017014763.1:c.-245-9_-245-8del	XP_016870252.1:n.-245-9_-245-8del
XR_001746315.1:n.419-9_419-8del
NM_004560.4:c.176-9_176-8del MANE Select	NP_004551.2:n.176-9_176-8del
NM_001318204.2:c.176-9_176-8del	NP_001305133.1:n.176-9_176-8del