Canonical Allele Identifier: CA373793122

Gene: ROR2

Linked Data

• dbSNP Id: rs1374283163
• gnomAD v2: 9-94486010-C-G
• gnomAD v4: 9-91723728-C-G
• MyVariant Identifiers: chr9:g.94486010C>G (hg19) ; chr9:g.91723728C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723728C>G , CM000671.2:g.91723728C>G	GRCh38
NC_000009.11:g.94486010C>G , CM000671.1:g.94486010C>G	GRCh37
NC_000009.10:g.93525831C>G	NCBI36
NG_008089.1:g.231435G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2766G>C MANE Select	ENSP00000364860.3:p.Glu922Asp
ENST00000375708.3:c.2766G>C	ENSP00000364860.3:p.Glu922Asp
ENST00000375715.5:c.1920+426G>C	ENSP00000364867.1:n.1920+426G>C
ENST00000550066.5:n.3234G>C
NM_004560.3:c.2766G>C	NP_004551.2:p.Glu922Asp
XM_005252008.3:c.2346G>C	XP_005252065.1:p.Glu782Asp
XM_005252009.3:c.1563G>C	XP_005252066.1:p.Glu521Asp
XM_006717121.2:c.2346G>C	XP_006717184.1:p.Glu782Asp
XM_011518721.1:c.2346G>C	XP_011517023.1:p.Glu782Asp
XM_005252008.4:c.2346G>C	XP_005252065.1:p.Glu782Asp
XM_006717121.3:c.2346G>C	XP_006717184.1:p.Glu782Asp
XM_017014762.1:c.2757G>C	XP_016870251.1:p.Glu919Asp
XM_017014763.1:c.2346G>C	XP_016870252.1:p.Glu782Asp
NM_004560.4:c.2766G>C MANE Select	NP_004551.2:p.Glu922Asp