Canonical Allele Identifier: CA10630558
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 367520
ClinVar RCV Id: RCV000264551 RCV000324615
dbSNP Id: rs184095609
gnomAD v2: 9-94712305-C-A
gnomAD v3: 9-91950023-C-A
gnomAD v4: 9-91950023-C-A
MyVariant Identifiers: chr9:g.94712305C>A (hg19) chr9:g.91950023C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91950023C>A , CM000671.2:g.91950023C>A GRCh38
NC_000009.11:g.94712305C>A , CM000671.1:g.94712305C>A GRCh37
NC_000009.10:g.93752126C>A NCBI36
NG_008089.1:g.5140G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.-60G>T MANE Select ENSP00000364860.3:n.-60G>T
ENST00000375708.3:c.-60G>T ENSP00000364860.3:n.-60G>T
NM_004560.3:c.-60G>T NP_004551.2:n.-60G>T
NM_001318204.1:c.-60G>T NP_001305133.1:n.-60G>T
XR_001746315.1:n.184G>T
NM_004560.4:c.-60G>T MANE Select NP_004551.2:n.-60G>T
NM_001318204.2:c.-60G>T NP_001305133.1:n.-60G>T
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