Canonical Allele Identifier: CA373793092

Gene: ROR2

Linked Data

• ClinVar Variation Id: 912788
• ClinVar RCV Id: RCV001166154 ; RCV001166155
• dbSNP Id: rs199855010
• gnomAD v4: 9-91723712-C-T
• MyVariant Identifiers: chr9:g.94485994C>T (hg19) ; chr9:g.91723712C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723712C>T , CM000671.2:g.91723712C>T	GRCh38
NC_000009.11:g.94485994C>T , CM000671.1:g.94485994C>T	GRCh37
NC_000009.10:g.93525815C>T	NCBI36
NG_008089.1:g.231451G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2782G>A MANE Select	ENSP00000364860.3:p.Asp928Asn
ENST00000375708.3:c.2782G>A	ENSP00000364860.3:p.Asp928Asn
ENST00000375715.5:c.1920+442G>A	ENSP00000364867.1:n.1920+442G>A
ENST00000550066.5:n.3250G>A
NM_004560.3:c.2782G>A	NP_004551.2:p.Asp928Asn
XM_005252008.3:c.2362G>A	XP_005252065.1:p.Asp788Asn
XM_005252009.3:c.1579G>A	XP_005252066.1:p.Asp527Asn
XM_006717121.2:c.2362G>A	XP_006717184.1:p.Asp788Asn
XM_011518721.1:c.2362G>A	XP_011517023.1:p.Asp788Asn
XM_005252008.4:c.2362G>A	XP_005252065.1:p.Asp788Asn
XM_006717121.3:c.2362G>A	XP_006717184.1:p.Asp788Asn
XM_017014762.1:c.2773G>A	XP_016870251.1:p.Asp925Asn
XM_017014763.1:c.2362G>A	XP_016870252.1:p.Asp788Asn
NM_004560.4:c.2782G>A MANE Select	NP_004551.2:p.Asp928Asn