Canonical Allele Identifier: CA10634110
Gene: ROR2 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.91950084T>G
GRCh37 chr9:g.94712366T>G
gnomAD v2:
9:94712366 T / G
gnomAD v3:
9:91950084 T / G
gnomAD v4:
chr9-91950084-T-G
Joint Max Group AF 0.00058979 (AFR)
Genomes Max Group AF 0.00056208 (AFR)
Exomes Max Group AF 0.00038744 (AFR)
ClinVar RCV:
RCV000280726
RCV000349772
ClinVar Variation:
367523
dbSNP:
555789981
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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
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