Canonical Allele Identifier: CA5121157
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 367519
ClinVar RCV Id: RCV000309212 RCV000359270
dbSNP Id: rs756061621
ExAC: 9:94712281 T / C
gnomAD v2: 9-94712281-T-C
gnomAD v3: 9-91949999-T-C
gnomAD v4: 9-91949999-T-C
MyVariant Identifiers: chr9:g.94712281T>C (hg19) chr9:g.91949999T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91949999T>C , CM000671.2:g.91949999T>C GRCh38
NC_000009.11:g.94712281T>C , CM000671.1:g.94712281T>C GRCh37
NC_000009.10:g.93752102T>C NCBI36
NG_008089.1:g.5164A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.-36A>G MANE Select ENSP00000364860.3:n.-36A>G
ENST00000375708.3:c.-36A>G ENSP00000364860.3:n.-36A>G
NM_004560.3:c.-36A>G NP_004551.2:n.-36A>G
NM_001318204.1:c.-36A>G NP_001305133.1:n.-36A>G
XR_001746315.1:n.208A>G
NM_004560.4:c.-36A>G MANE Select NP_004551.2:n.-36A>G
NM_001318204.2:c.-36A>G NP_001305133.1:n.-36A>G
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