Canonical Allele Identifier: CA5121083
Gene: ROR2 HGNC NCBI

Linked Data

dbSNP Id: rs772202601
gnomAD v4: 9-91757526-T-C

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