Canonical Allele Identifier: CA373793208

Gene: ROR2

Linked Data

• ClinVar Variation Id: 2636401
• ClinVar RCV Id: RCV004534413
• gnomAD v4: 9-91723765-T-C
• MyVariant Identifiers: chr9:g.94486047T>C (hg19) ; chr9:g.91723765T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723765T>C , CM000671.2:g.91723765T>C	GRCh38
NC_000009.11:g.94486047T>C , CM000671.1:g.94486047T>C	GRCh37
NC_000009.10:g.93525868T>C	NCBI36
NG_008089.1:g.231398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2729A>G MANE Select	ENSP00000364860.3:p.Gln910Arg
ENST00000375708.3:c.2729A>G	ENSP00000364860.3:p.Gln910Arg
ENST00000375715.5:c.1920+389A>G	ENSP00000364867.1:n.1920+389A>G
ENST00000550066.5:n.3197A>G
NM_004560.3:c.2729A>G	NP_004551.2:p.Gln910Arg
XM_005252008.3:c.2309A>G	XP_005252065.1:p.Gln770Arg
XM_005252009.3:c.1526A>G	XP_005252066.1:p.Gln509Arg
XM_006717121.2:c.2309A>G	XP_006717184.1:p.Gln770Arg
XM_011518721.1:c.2309A>G	XP_011517023.1:p.Gln770Arg
XM_005252008.4:c.2309A>G	XP_005252065.1:p.Gln770Arg
XM_006717121.3:c.2309A>G	XP_006717184.1:p.Gln770Arg
XM_017014762.1:c.2720A>G	XP_016870251.1:p.Gln907Arg
XM_017014763.1:c.2309A>G	XP_016870252.1:p.Gln770Arg
NM_004560.4:c.2729A>G MANE Select	NP_004551.2:p.Gln910Arg