Canonical Allele Identifier: CA118707
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7305
ClinVar RCV Id: RCV000007728
dbSNP Id: rs104894122
MyVariant Identifiers: chr9:g.94486530C>T (hg19) chr9:g.91724248C>T (hg38)
PubMed: PMID:641944 PMID:10700182
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91724248C>T , CM000671.2:g.91724248C>T GRCh38
NC_000009.11:g.94486530C>T , CM000671.1:g.94486530C>T GRCh37
NC_000009.10:g.93526351C>T NCBI36
NG_008089.1:g.230915G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375708.4:c.2246G>A MANE Select ENSP00000364860.3:p.Trp749Ter
ENST00000375708.3:c.2246G>A ENSP00000364860.3:p.Trp749Ter
ENST00000375715.5:c.1826G>A ENSP00000364867.1:p.Trp609Ter
ENST00000550066.5:n.2714G>A
NM_004560.3:c.2246G>A NP_004551.2:p.Trp749Ter
XM_005252008.3:c.1826G>A XP_005252065.1:p.Trp609Ter
XM_005252009.3:c.1043G>A XP_005252066.1:p.Trp348Ter
XM_006717121.2:c.1826G>A XP_006717184.1:p.Trp609Ter
XM_011518721.1:c.1826G>A XP_011517023.1:p.Trp609Ter
XM_005252008.4:c.1826G>A XP_005252065.1:p.Trp609Ter
XM_006717121.3:c.1826G>A XP_006717184.1:p.Trp609Ter
XM_017014762.1:c.2237G>A XP_016870251.1:p.Trp746Ter
XM_017014763.1:c.1826G>A XP_016870252.1:p.Trp609Ter
NM_004560.4:c.2246G>A MANE Select NP_004551.2:p.Trp749Ter
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