Canonical Allele Identifier: CA5120336

Gene: ROR2

Linked Data

• ClinVar Variation Id: 747534
• ClinVar RCV Id: RCV000924252
• dbSNP Id: rs146866887
• ExAC: 9:94486094 A / C
• gnomAD v2: 9-94486094-A-C
• gnomAD v3: 9-91723812-A-C
• gnomAD v4: 9-91723812-A-C
• MyVariant Identifiers: chr9:g.94486094A>C (hg19) ; chr9:g.91723812A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723812A>C , CM000671.2:g.91723812A>C	GRCh38
NC_000009.11:g.94486094A>C , CM000671.1:g.94486094A>C	GRCh37
NC_000009.10:g.93525915A>C	NCBI36
NG_008089.1:g.231351T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2682T>G MANE Select	ENSP00000364860.3:p.Ala894=
ENST00000375708.3:c.2682T>G	ENSP00000364860.3:p.Ala894=
ENST00000375715.5:c.1920+342T>G	ENSP00000364867.1:n.1920+342T>G
ENST00000550066.5:n.3150T>G
NM_004560.3:c.2682T>G	NP_004551.2:p.Ala894=
XM_005252008.3:c.2262T>G	XP_005252065.1:p.Ala754=
XM_005252009.3:c.1479T>G	XP_005252066.1:p.Ala493=
XM_006717121.2:c.2262T>G	XP_006717184.1:p.Ala754=
XM_011518721.1:c.2262T>G	XP_011517023.1:p.Ala754=
XM_005252008.4:c.2262T>G	XP_005252065.1:p.Ala754=
XM_006717121.3:c.2262T>G	XP_006717184.1:p.Ala754=
XM_017014762.1:c.2673T>G	XP_016870251.1:p.Ala891=
XM_017014763.1:c.2262T>G	XP_016870252.1:p.Ala754=
NM_004560.4:c.2682T>G MANE Select	NP_004551.2:p.Ala894=