Canonical Allele Identifier: CA373799245
Gene: ROR2 HGNC NCBI

Linked Data

gnomAD v4: 9-91726542-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91726542T>C , CM000671.2:g.91726542T>C GRCh38
NC_000009.11:g.94488824T>C , CM000671.1:g.94488824T>C GRCh37
NC_000009.10:g.93528645T>C NCBI36
NG_008089.1:g.228621A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.1385A>G MANE Select ENSP00000364860.3:p.Gln462Arg
ENST00000375708.3:c.1385A>G ENSP00000364860.3:p.Gln462Arg
ENST00000375715.5:c.965A>G ENSP00000364867.1:p.Gln322Arg
ENST00000550066.5:n.1853A>G
NM_004560.3:c.1385A>G NP_004551.2:p.Gln462Arg
XM_005252008.3:c.965A>G XP_005252065.1:p.Gln322Arg
XM_005252009.3:c.182A>G XP_005252066.1:p.Gln61Arg
XM_006717121.2:c.965A>G XP_006717184.1:p.Gln322Arg
XM_011518721.1:c.965A>G XP_011517023.1:p.Gln322Arg
NM_001318204.1:c.*52A>G NP_001305133.1:n.*52A>G
XM_005252008.4:c.965A>G XP_005252065.1:p.Gln322Arg
XM_006717121.3:c.965A>G XP_006717184.1:p.Gln322Arg
XM_017014762.1:c.1376A>G XP_016870251.1:p.Gln459Arg
XM_017014763.1:c.965A>G XP_016870252.1:p.Gln322Arg
XR_001746315.1:n.1594A>G
NM_004560.4:c.1385A>G MANE Select NP_004551.2:p.Gln462Arg
NM_001318204.2:c.*52A>G NP_001305133.1:n.*52A>G