Canonical Allele Identifier: CA10634110

Gene: ROR2

Linked Data

• ClinVar Variation Id: 367523
• ClinVar RCV Id: RCV000280726 ; RCV000349772
• dbSNP Id: rs555789981
• gnomAD v2: 9-94712366-T-G
• gnomAD v3: 9-91950084-T-G
• gnomAD v4: 9-91950084-T-G
• MyVariant Identifiers: chr9:g.94712366T>G (hg19) ; chr9:g.91950084T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91950084T>G , CM000671.2:g.91950084T>G	GRCh38
NC_000009.11:g.94712366T>G , CM000671.1:g.94712366T>G	GRCh37
NC_000009.10:g.93752187T>G	NCBI36
NG_008089.1:g.5079A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.-121A>C MANE Select	ENSP00000364860.3:n.-121A>C
ENST00000375708.3:c.-121A>C	ENSP00000364860.3:n.-121A>C
NM_004560.3:c.-121A>C	NP_004551.2:n.-121A>C
NM_001318204.1:c.-121A>C	NP_001305133.1:n.-121A>C
XR_001746315.1:n.123A>C
NM_004560.4:c.-121A>C MANE Select	NP_004551.2:n.-121A>C
NM_001318204.2:c.-121A>C	NP_001305133.1:n.-121A>C