Canonical Allele Identifier: CA373840570

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519620A>C (hg19) ; chr9:g.91757338A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757338A>C , CM000671.2:g.91757338A>C	GRCh38
NC_000009.11:g.94519620A>C , CM000671.1:g.94519620A>C	GRCh37
NC_000009.10:g.93559441A>C	NCBI36
NG_008089.1:g.197825T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.397T>G MANE Select	ENSP00000364860.3:p.Tyr133Asp
ENST00000375708.3:c.397T>G	ENSP00000364860.3:p.Tyr133Asp
ENST00000375715.5:c.-24T>G	ENSP00000364867.1:n.-24T>G
ENST00000495386.5:n.660T>G
ENST00000548585.2:n.172+91T>G
ENST00000550066.5:n.865T>G
NM_004560.3:c.397T>G	NP_004551.2:p.Tyr133Asp
XM_005252008.3:c.-24T>G	XP_005252065.1:n.-24T>G
XM_006717121.2:c.-24T>G	XP_006717184.1:n.-24T>G
XM_011518721.1:c.-24T>G	XP_011517023.1:n.-24T>G
NM_001318204.1:c.397T>G	NP_001305133.1:p.Tyr133Asp
XM_005252008.4:c.-24T>G	XP_005252065.1:n.-24T>G
XM_006717121.3:c.-24T>G	XP_006717184.1:n.-24T>G
XM_017014762.1:c.388T>G	XP_016870251.1:p.Tyr130Asp
XM_017014763.1:c.-24T>G	XP_016870252.1:n.-24T>G
XR_001746315.1:n.640T>G
NM_004560.4:c.397T>G MANE Select	NP_004551.2:p.Tyr133Asp
NM_001318204.2:c.397T>G	NP_001305133.1:p.Tyr133Asp