Canonical Allele Identifier: CA373800031

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91730988C>G , CM000671.2:g.91730988C>G	GRCh38
NC_000009.11:g.94493270C>G , CM000671.1:g.94493270C>G	GRCh37
NC_000009.10:g.93533091C>G	NCBI36
NG_008089.1:g.224175G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1105G>C MANE Select	ENSP00000364860.3:p.Gly369Arg
ENST00000375708.3:c.1105G>C	ENSP00000364860.3:p.Gly369Arg
ENST00000375715.5:c.685G>C	ENSP00000364867.1:p.Gly229Arg
ENST00000550066.5:n.1573G>C
NM_004560.3:c.1105G>C	NP_004551.2:p.Gly369Arg
XM_005252008.3:c.685G>C	XP_005252065.1:p.Gly229Arg
XM_005252009.3:c.-65G>C	XP_005252066.1:n.-65G>C
XM_006717121.2:c.685G>C	XP_006717184.1:p.Gly229Arg
XM_011518721.1:c.685G>C	XP_011517023.1:p.Gly229Arg
NM_001318204.1:c.1105G>C	NP_001305133.1:p.Gly369Arg
XM_005252008.4:c.685G>C	XP_005252065.1:p.Gly229Arg
XM_006717121.3:c.685G>C	XP_006717184.1:p.Gly229Arg
XM_017014762.1:c.1096G>C	XP_016870251.1:p.Gly366Arg
XM_017014763.1:c.685G>C	XP_016870252.1:p.Gly229Arg
XR_001746315.1:n.1348G>C
NM_004560.4:c.1105G>C MANE Select	NP_004551.2:p.Gly369Arg
NM_001318204.2:c.1105G>C	NP_001305133.1:p.Gly369Arg