Canonical Allele Identifier: CA272467

Gene: ROR2

Linked Data

• ClinVar Variation Id: 159812
• ClinVar RCV Id: RCV000147383 ; RCV000374484 ; RCV000886960
• dbSNP Id: rs144549032
• ExAC: 9:94486817 C / T
• gnomAD v2: 9-94486817-C-T
• gnomAD v3: 9-91724535-C-T
• gnomAD v4: 9-91724535-C-T
• MyVariant Identifiers: chr9:g.94486817C>T (hg19) ; chr9:g.91724535C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724535C>T , CM000671.2:g.91724535C>T	GRCh38
NC_000009.11:g.94486817C>T , CM000671.1:g.94486817C>T	GRCh37
NC_000009.10:g.93526638C>T	NCBI36
NG_008089.1:g.230628G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1959G>A MANE Select	ENSP00000364860.3:p.Leu653=
ENST00000375708.3:c.1959G>A	ENSP00000364860.3:p.Leu653=
ENST00000375715.5:c.1539G>A	ENSP00000364867.1:p.Leu513=
ENST00000550066.5:n.2427G>A
NM_004560.3:c.1959G>A	NP_004551.2:p.Leu653=
XM_005252008.3:c.1539G>A	XP_005252065.1:p.Leu513=
XM_005252009.3:c.756G>A	XP_005252066.1:p.Leu252=
XM_006717121.2:c.1539G>A	XP_006717184.1:p.Leu513=
XM_011518721.1:c.1539G>A	XP_011517023.1:p.Leu513=
XM_005252008.4:c.1539G>A	XP_005252065.1:p.Leu513=
XM_006717121.3:c.1539G>A	XP_006717184.1:p.Leu513=
XM_017014762.1:c.1950G>A	XP_016870251.1:p.Leu650=
XM_017014763.1:c.1539G>A	XP_016870252.1:p.Leu513=
NM_004560.4:c.1959G>A MANE Select	NP_004551.2:p.Leu653=