Canonical Allele Identifier: CA373799399

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488887C>G (hg19) ; chr9:g.91726605C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726605C>G , CM000671.2:g.91726605C>G	GRCh38
NC_000009.11:g.94488887C>G , CM000671.1:g.94488887C>G	GRCh37
NC_000009.10:g.93528708C>G	NCBI36
NG_008089.1:g.228558G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1322G>C MANE Select	ENSP00000364860.3:p.Arg441Pro
ENST00000375708.3:c.1322G>C	ENSP00000364860.3:p.Arg441Pro
ENST00000375715.5:c.902G>C	ENSP00000364867.1:p.Arg301Pro
ENST00000550066.5:n.1790G>C
NM_004560.3:c.1322G>C	NP_004551.2:p.Arg441Pro
XM_005252008.3:c.902G>C	XP_005252065.1:p.Arg301Pro
XM_005252009.3:c.119G>C	XP_005252066.1:p.Arg40Pro
XM_006717121.2:c.902G>C	XP_006717184.1:p.Arg301Pro
XM_011518721.1:c.902G>C	XP_011517023.1:p.Arg301Pro
NM_001318204.1:c.1288G>C	NP_001305133.1:p.Gly430Arg
XM_005252008.4:c.902G>C	XP_005252065.1:p.Arg301Pro
XM_006717121.3:c.902G>C	XP_006717184.1:p.Arg301Pro
XM_017014762.1:c.1313G>C	XP_016870251.1:p.Arg438Pro
XM_017014763.1:c.902G>C	XP_016870252.1:p.Arg301Pro
XR_001746315.1:n.1531G>C
NM_004560.4:c.1322G>C MANE Select	NP_004551.2:p.Arg441Pro
NM_001318204.2:c.1288G>C	NP_001305133.1:p.Gly430Arg