Canonical Allele Identifier: CA5120323

Gene: ROR2

Linked Data

• ClinVar Variation Id: 1443599
• ClinVar RCV Id: RCV001955687 ; RCV004043644
• dbSNP Id: rs778811682
• ExAC: 9:94486051 C / T
• gnomAD v2: 9-94486051-C-T
• gnomAD v4: 9-91723769-C-T
• COSMIC: COSM1132437
• MyVariant Identifiers: chr9:g.94486051C>T (hg19) ; chr9:g.91723769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723769C>T , CM000671.2:g.91723769C>T	GRCh38
NC_000009.11:g.94486051C>T , CM000671.1:g.94486051C>T	GRCh37
NC_000009.10:g.93525872C>T	NCBI36
NG_008089.1:g.231394G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2725G>A MANE Select	ENSP00000364860.3:p.Val909Met
ENST00000375708.3:c.2725G>A	ENSP00000364860.3:p.Val909Met
ENST00000375715.5:c.1920+385G>A	ENSP00000364867.1:n.1920+385G>A
ENST00000550066.5:n.3193G>A
NM_004560.3:c.2725G>A	NP_004551.2:p.Val909Met
XM_005252008.3:c.2305G>A	XP_005252065.1:p.Val769Met
XM_005252009.3:c.1522G>A	XP_005252066.1:p.Val508Met
XM_006717121.2:c.2305G>A	XP_006717184.1:p.Val769Met
XM_011518721.1:c.2305G>A	XP_011517023.1:p.Val769Met
XM_005252008.4:c.2305G>A	XP_005252065.1:p.Val769Met
XM_006717121.3:c.2305G>A	XP_006717184.1:p.Val769Met
XM_017014762.1:c.2716G>A	XP_016870251.1:p.Val906Met
XM_017014763.1:c.2305G>A	XP_016870252.1:p.Val769Met
NM_004560.4:c.2725G>A MANE Select	NP_004551.2:p.Val909Met