Canonical Allele Identifier: CA195325697

Gene: ROR2

Linked Data

• ClinVar Variation Id: 2098970
• ClinVar RCV Id: RCV003022766
• dbSNP Id: rs371810993
• MyVariant Identifiers: chr9:g.94488884C>T (hg19) ; chr9:g.91726602C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726602C>T , CM000671.2:g.91726602C>T	GRCh38
NC_000009.11:g.94488884C>T , CM000671.1:g.94488884C>T	GRCh37
NC_000009.10:g.93528705C>T	NCBI36
NG_008089.1:g.228561G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1325G>A MANE Select	ENSP00000364860.3:p.Arg442Gln
ENST00000375708.3:c.1325G>A	ENSP00000364860.3:p.Arg442Gln
ENST00000375715.5:c.905G>A	ENSP00000364867.1:p.Arg302Gln
ENST00000550066.5:n.1793G>A
NM_004560.3:c.1325G>A	NP_004551.2:p.Arg442Gln
XM_005252008.3:c.905G>A	XP_005252065.1:p.Arg302Gln
XM_005252009.3:c.122G>A	XP_005252066.1:p.Arg41Gln
XM_006717121.2:c.905G>A	XP_006717184.1:p.Arg302Gln
XM_011518721.1:c.905G>A	XP_011517023.1:p.Arg302Gln
NM_001318204.1:c.1291G>A	NP_001305133.1:p.Asp431Asn
XM_005252008.4:c.905G>A	XP_005252065.1:p.Arg302Gln
XM_006717121.3:c.905G>A	XP_006717184.1:p.Arg302Gln
XM_017014762.1:c.1316G>A	XP_016870251.1:p.Arg439Gln
XM_017014763.1:c.905G>A	XP_016870252.1:p.Arg302Gln
XR_001746315.1:n.1534G>A
NM_004560.4:c.1325G>A MANE Select	NP_004551.2:p.Arg442Gln
NM_001318204.2:c.1291G>A	NP_001305133.1:p.Asp431Asn