Canonical Allele Identifier: CA10634450
Gene: ROR2 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.91723142G>A
GRCh37 chr9:g.94485424G>A
gnomAD v2:
9:94485424 G / A
gnomAD v3:
9:91723142 G / A
gnomAD v4:
chr9-91723142-G-A
Joint Max Group AF 0.00421405 (SAS)
Genomes Max Group AF 0.00448749 (SAS)
ClinVar Allele:
319924
ClinVar RCV:
RCV000320989
RCV000375734
ClinVar Variation:
367488
dbSNP:
367760102
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91723142G>A , CM000671.2:g.91723142G>A GRCh38
NC_000009.11:g.94485424G>A , CM000671.1:g.94485424G>A GRCh37
NC_000009.10:g.93525245G>A NCBI36
NG_008089.1:g.232021C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.*520C>T MANE Select ENSP00000364860.3:n.*520C>T
ENST00000375708.3:c.*520C>T ENSP00000364860.3:n.*520C>T
ENST00000375715.5:c.1921-562C>T ENSP00000364867.1:n.1921-562C>T
ENST00000550066.5:n.3820C>T
NM_004560.3:c.*520C>T NP_004551.2:n.*520C>T
XM_005252008.3:c.*520C>T XP_005252065.1:n.*520C>T
XM_005252009.3:c.*520C>T XP_005252066.1:n.*520C>T
XM_006717121.2:c.*520C>T XP_006717184.1:n.*520C>T
XM_011518721.1:c.*520C>T XP_011517023.1:n.*520C>T
XM_005252008.4:c.*520C>T XP_005252065.1:n.*520C>T
XM_006717121.3:c.*520C>T XP_006717184.1:n.*520C>T
XM_017014762.1:c.*520C>T XP_016870251.1:n.*520C>T
XM_017014763.1:c.*520C>T XP_016870252.1:n.*520C>T
NM_004560.4:c.*520C>T MANE Select NP_004551.2:n.*520C>T
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