Canonical Allele Identifier: CA373797883

Gene: ROR2

Linked Data

• ClinVar Variation Id: 1382727
• ClinVar RCV Id: RCV001890505 ; RCV002482648
• dbSNP Id: rs1489863862
• gnomAD v2: 9-94487137-G-T
• gnomAD v3: 9-91724855-G-T
• gnomAD v4: 9-91724855-G-T
• COSMIC: COSM1264487
• MyVariant Identifiers: chr9:g.94487137G>T (hg19) ; chr9:g.91724855G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724855G>T , CM000671.2:g.91724855G>T	GRCh38
NC_000009.11:g.94487137G>T , CM000671.1:g.94487137G>T	GRCh37
NC_000009.10:g.93526958G>T	NCBI36
NG_008089.1:g.230308C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1639C>A MANE Select	ENSP00000364860.3:p.Gln547Lys
ENST00000375708.3:c.1639C>A	ENSP00000364860.3:p.Gln547Lys
ENST00000375715.5:c.1219C>A	ENSP00000364867.1:p.Gln407Lys
ENST00000550066.5:n.2107C>A
NM_004560.3:c.1639C>A	NP_004551.2:p.Gln547Lys
XM_005252008.3:c.1219C>A	XP_005252065.1:p.Gln407Lys
XM_005252009.3:c.436C>A	XP_005252066.1:p.Gln146Lys
XM_006717121.2:c.1219C>A	XP_006717184.1:p.Gln407Lys
XM_011518721.1:c.1219C>A	XP_011517023.1:p.Gln407Lys
XM_005252008.4:c.1219C>A	XP_005252065.1:p.Gln407Lys
XM_006717121.3:c.1219C>A	XP_006717184.1:p.Gln407Lys
XM_017014762.1:c.1630C>A	XP_016870251.1:p.Gln544Lys
XM_017014763.1:c.1219C>A	XP_016870252.1:p.Gln407Lys
NM_004560.4:c.1639C>A MANE Select	NP_004551.2:p.Gln547Lys