Canonical Allele Identifier: CA373793314
Gene: ROR2 HGNC NCBI

Linked Data

gnomAD v4: 9-91723816-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91723816C>T , CM000671.2:g.91723816C>T GRCh38
NC_000009.11:g.94486098C>T , CM000671.1:g.94486098C>T GRCh37
NC_000009.10:g.93525919C>T NCBI36
NG_008089.1:g.231347G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.2678G>A MANE Select ENSP00000364860.3:p.Gly893Asp
ENST00000375708.3:c.2678G>A ENSP00000364860.3:p.Gly893Asp
ENST00000375715.5:c.1920+338G>A ENSP00000364867.1:n.1920+338G>A
ENST00000550066.5:n.3146G>A
NM_004560.3:c.2678G>A NP_004551.2:p.Gly893Asp
XM_005252008.3:c.2258G>A XP_005252065.1:p.Gly753Asp
XM_005252009.3:c.1475G>A XP_005252066.1:p.Gly492Asp
XM_006717121.2:c.2258G>A XP_006717184.1:p.Gly753Asp
XM_011518721.1:c.2258G>A XP_011517023.1:p.Gly753Asp
XM_005252008.4:c.2258G>A XP_005252065.1:p.Gly753Asp
XM_006717121.3:c.2258G>A XP_006717184.1:p.Gly753Asp
XM_017014762.1:c.2669G>A XP_016870251.1:p.Gly890Asp
XM_017014763.1:c.2258G>A XP_016870252.1:p.Gly753Asp
NM_004560.4:c.2678G>A MANE Select NP_004551.2:p.Gly893Asp