Canonical Allele Identifier: CA5120334

Gene: ROR2

Linked Data

• dbSNP Id: rs766587026
• ExAC: 9:94486084 G / C
• gnomAD v2: 9-94486084-G-C
• gnomAD v4: 9-91723802-G-C
• MyVariant Identifiers: chr9:g.94486084G>C (hg19) ; chr9:g.91723802G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723802G>C , CM000671.2:g.91723802G>C	GRCh38
NC_000009.11:g.94486084G>C , CM000671.1:g.94486084G>C	GRCh37
NC_000009.10:g.93525905G>C	NCBI36
NG_008089.1:g.231361C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2692C>G MANE Select	ENSP00000364860.3:p.Gln898Glu
ENST00000375708.3:c.2692C>G	ENSP00000364860.3:p.Gln898Glu
ENST00000375715.5:c.1920+352C>G	ENSP00000364867.1:n.1920+352C>G
ENST00000550066.5:n.3160C>G
NM_004560.3:c.2692C>G	NP_004551.2:p.Gln898Glu
XM_005252008.3:c.2272C>G	XP_005252065.1:p.Gln758Glu
XM_005252009.3:c.1489C>G	XP_005252066.1:p.Gln497Glu
XM_006717121.2:c.2272C>G	XP_006717184.1:p.Gln758Glu
XM_011518721.1:c.2272C>G	XP_011517023.1:p.Gln758Glu
XM_005252008.4:c.2272C>G	XP_005252065.1:p.Gln758Glu
XM_006717121.3:c.2272C>G	XP_006717184.1:p.Gln758Glu
XM_017014762.1:c.2683C>G	XP_016870251.1:p.Gln895Glu
XM_017014763.1:c.2272C>G	XP_016870252.1:p.Gln758Glu
NM_004560.4:c.2692C>G MANE Select	NP_004551.2:p.Gln898Glu