Canonical Allele Identifier: CA10634450
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 367488
dbSNP Id: rs367760102
gnomAD v2: 9-94485424-G-A
gnomAD v3: 9-91723142-G-A
gnomAD v4: 9-91723142-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91723142G>A , CM000671.2:g.91723142G>A GRCh38
NC_000009.11:g.94485424G>A , CM000671.1:g.94485424G>A GRCh37
NC_000009.10:g.93525245G>A NCBI36
NG_008089.1:g.232021C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.*520C>T MANE Select ENSP00000364860.3:n.*520C>T
ENST00000375708.3:c.*520C>T ENSP00000364860.3:n.*520C>T
ENST00000375715.5:c.1921-562C>T ENSP00000364867.1:n.1921-562C>T
ENST00000550066.5:n.3820C>T
NM_004560.3:c.*520C>T NP_004551.2:n.*520C>T
XM_005252008.3:c.*520C>T XP_005252065.1:n.*520C>T
XM_005252009.3:c.*520C>T XP_005252066.1:n.*520C>T
XM_006717121.2:c.*520C>T XP_006717184.1:n.*520C>T
XM_011518721.1:c.*520C>T XP_011517023.1:n.*520C>T
XM_005252008.4:c.*520C>T XP_005252065.1:n.*520C>T
XM_006717121.3:c.*520C>T XP_006717184.1:n.*520C>T
XM_017014762.1:c.*520C>T XP_016870251.1:n.*520C>T
XM_017014763.1:c.*520C>T XP_016870252.1:n.*520C>T
NM_004560.4:c.*520C>T MANE Select NP_004551.2:n.*520C>T