Canonical Allele Identifier: CA1863921283

Gene: ROR2

Linked Data

• dbSNP Id: rs2230578

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723646C>G , CM000671.2:g.91723646C>G	GRCh38
NC_000009.11:g.94485928C>G , CM000671.1:g.94485928C>G	GRCh37
NC_000009.10:g.93525749C>G	NCBI36
NG_008089.1:g.231517G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*16G>C MANE Select	ENSP00000364860.3:n.*16G>C
ENST00000375708.3:c.*16G>C	ENSP00000364860.3:n.*16G>C
ENST00000375715.5:c.1920+508G>C	ENSP00000364867.1:n.1920+508G>C
ENST00000550066.5:n.3316G>C
NM_004560.3:c.*16G>C	NP_004551.2:n.*16G>C
XM_005252008.3:c.*16G>C	XP_005252065.1:n.*16G>C
XM_005252009.3:c.*16G>C	XP_005252066.1:n.*16G>C
XM_006717121.2:c.*16G>C	XP_006717184.1:n.*16G>C
XM_011518721.1:c.*16G>C	XP_011517023.1:n.*16G>C
XM_005252008.4:c.*16G>C	XP_005252065.1:n.*16G>C
XM_006717121.3:c.*16G>C	XP_006717184.1:n.*16G>C
XM_017014762.1:c.*16G>C	XP_016870251.1:n.*16G>C
XM_017014763.1:c.*16G>C	XP_016870252.1:n.*16G>C
NM_004560.4:c.*16G>C MANE Select	NP_004551.2:n.*16G>C