Canonical Allele Identifier: CA5120497

Gene: ROR2

Linked Data

• ClinVar Variation Id: 2241163
• ClinVar RCV Id: RCV002747340
• dbSNP Id: rs766445029
• ExAC: 9:94486711 C / T
• gnomAD v2: 9-94486711-C-T
• gnomAD v4: 9-91724429-C-T
• COSMIC: COSM4758929
• MyVariant Identifiers: chr9:g.94486711C>T (hg19) ; chr9:g.91724429C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724429C>T , CM000671.2:g.91724429C>T	GRCh38
NC_000009.11:g.94486711C>T , CM000671.1:g.94486711C>T	GRCh37
NC_000009.10:g.93526532C>T	NCBI36
NG_008089.1:g.230734G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2065G>A MANE Select	ENSP00000364860.3:p.Gly689Ser
ENST00000375708.3:c.2065G>A	ENSP00000364860.3:p.Gly689Ser
ENST00000375715.5:c.1645G>A	ENSP00000364867.1:p.Gly549Ser
ENST00000550066.5:n.2533G>A
NM_004560.3:c.2065G>A	NP_004551.2:p.Gly689Ser
XM_005252008.3:c.1645G>A	XP_005252065.1:p.Gly549Ser
XM_005252009.3:c.862G>A	XP_005252066.1:p.Gly288Ser
XM_006717121.2:c.1645G>A	XP_006717184.1:p.Gly549Ser
XM_011518721.1:c.1645G>A	XP_011517023.1:p.Gly549Ser
XM_005252008.4:c.1645G>A	XP_005252065.1:p.Gly549Ser
XM_006717121.3:c.1645G>A	XP_006717184.1:p.Gly549Ser
XM_017014762.1:c.2056G>A	XP_016870251.1:p.Gly686Ser
XM_017014763.1:c.1645G>A	XP_016870252.1:p.Gly549Ser
NM_004560.4:c.2065G>A MANE Select	NP_004551.2:p.Gly689Ser