Canonical Allele Identifier: CA466339030

Gene: ROR2

Linked Data

• ClinVar Variation Id: 2748345
• ClinVar RCV Id: RCV003565963
• MyVariant Identifiers: chr9:g.94486709G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724427G>A , CM000671.2:g.91724427G>A	GRCh38
NC_000009.11:g.94486709G>A , CM000671.1:g.94486709G>A	GRCh37
NC_000009.10:g.93526530G>A	NCBI36
NG_008089.1:g.230736C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2067C>T MANE Select	ENSP00000364860.3:p.Gly689=
ENST00000375708.3:c.2067C>T	ENSP00000364860.3:p.Gly689=
ENST00000375715.5:c.1647C>T	ENSP00000364867.1:p.Gly549=
ENST00000550066.5:n.2535C>T
NM_004560.3:c.2067C>T	NP_004551.2:p.Gly689=
XM_005252008.3:c.1647C>T	XP_005252065.1:p.Gly549=
XM_005252009.3:c.864C>T	XP_005252066.1:p.Gly288=
XM_006717121.2:c.1647C>T	XP_006717184.1:p.Gly549=
XM_011518721.1:c.1647C>T	XP_011517023.1:p.Gly549=
XM_005252008.4:c.1647C>T	XP_005252065.1:p.Gly549=
XM_006717121.3:c.1647C>T	XP_006717184.1:p.Gly549=
XM_017014762.1:c.2058C>T	XP_016870251.1:p.Gly686=
XM_017014763.1:c.1647C>T	XP_016870252.1:p.Gly549=
NM_004560.4:c.2067C>T MANE Select	NP_004551.2:p.Gly689=