Canonical Allele Identifier: CA10627649

Gene: ROR2

Linked Data

• ClinVar Variation Id: 367494
• ClinVar RCV Id: RCV000363114 ; RCV000401563 ; RCV002480256
• dbSNP Id: rs774621355
• gnomAD v2: 9-94485809-C-A
• gnomAD v3: 9-91723527-C-A
• gnomAD v4: 9-91723527-C-A
• MyVariant Identifiers: chr9:g.94485809C>A (hg19) ; chr9:g.91723527C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723527C>A , CM000671.2:g.91723527C>A	GRCh38
NC_000009.11:g.94485809C>A , CM000671.1:g.94485809C>A	GRCh37
NC_000009.10:g.93525630C>A	NCBI36
NG_008089.1:g.231636G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*135G>T MANE Select	ENSP00000364860.3:n.*135G>T
ENST00000375708.3:c.*135G>T	ENSP00000364860.3:n.*135G>T
ENST00000375715.5:c.1920+627G>T	ENSP00000364867.1:n.1920+627G>T
ENST00000550066.5:n.3435G>T
NM_004560.3:c.*135G>T	NP_004551.2:n.*135G>T
XM_005252008.3:c.*135G>T	XP_005252065.1:n.*135G>T
XM_005252009.3:c.*135G>T	XP_005252066.1:n.*135G>T
XM_006717121.2:c.*135G>T	XP_006717184.1:n.*135G>T
XM_011518721.1:c.*135G>T	XP_011517023.1:n.*135G>T
XM_005252008.4:c.*135G>T	XP_005252065.1:n.*135G>T
XM_006717121.3:c.*135G>T	XP_006717184.1:n.*135G>T
XM_017014762.1:c.*135G>T	XP_016870251.1:n.*135G>T
XM_017014763.1:c.*135G>T	XP_016870252.1:n.*135G>T
NM_004560.4:c.*135G>T MANE Select	NP_004551.2:n.*135G>T