Canonical Allele Identifier: CA5121083

Gene: ROR2

Linked Data

• dbSNP Id: rs772202601
• ExAC: 9:94519808 T / C
• gnomAD v4: 9-91757526-T-C
• MyVariant Identifiers: chr9:g.94519808T>C (hg19) ; chr9:g.91757526T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757526T>C , CM000671.2:g.91757526T>C	GRCh38
NC_000009.11:g.94519808T>C , CM000671.1:g.94519808T>C	GRCh37
NC_000009.10:g.93559629T>C	NCBI36
NG_008089.1:g.197637A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.209A>G MANE Select	ENSP00000364860.3:p.Asn70Ser
ENST00000375708.3:c.209A>G	ENSP00000364860.3:p.Asn70Ser
ENST00000375715.5:c.-212A>G	ENSP00000364867.1:n.-212A>G
ENST00000495386.5:n.472A>G
ENST00000546883.1:n.411A>G
ENST00000548585.2:n.75A>G
ENST00000550066.5:n.677A>G
NM_004560.3:c.209A>G	NP_004551.2:p.Asn70Ser
XM_005252008.3:c.-212A>G	XP_005252065.1:n.-212A>G
XM_006717121.2:c.-212A>G	XP_006717184.1:n.-212A>G
XM_011518721.1:c.-212A>G	XP_011517023.1:n.-212A>G
NM_001318204.1:c.209A>G	NP_001305133.1:p.Asn70Ser
XM_005252008.4:c.-212A>G	XP_005252065.1:n.-212A>G
XM_006717121.3:c.-212A>G	XP_006717184.1:n.-212A>G
XM_017014762.1:c.200A>G	XP_016870251.1:p.Asn67Ser
XM_017014763.1:c.-212A>G	XP_016870252.1:n.-212A>G
XR_001746315.1:n.452A>G
NM_004560.4:c.209A>G MANE Select	NP_004551.2:p.Asn70Ser
NM_001318204.2:c.209A>G	NP_001305133.1:p.Asn70Ser