Canonical Allele Identifier: CA465995390

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94485974C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723692C>G , CM000671.2:g.91723692C>G	GRCh38
NC_000009.11:g.94485974C>G , CM000671.1:g.94485974C>G	GRCh37
NC_000009.10:g.93525795C>G	NCBI36
NG_008089.1:g.231471G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2802G>C MANE Select	ENSP00000364860.3:p.Val934=
ENST00000375708.3:c.2802G>C	ENSP00000364860.3:p.Val934=
ENST00000375715.5:c.1920+462G>C	ENSP00000364867.1:n.1920+462G>C
ENST00000550066.5:n.3270G>C
NM_004560.3:c.2802G>C	NP_004551.2:p.Val934=
XM_005252008.3:c.2382G>C	XP_005252065.1:p.Val794=
XM_005252009.3:c.1599G>C	XP_005252066.1:p.Val533=
XM_006717121.2:c.2382G>C	XP_006717184.1:p.Val794=
XM_011518721.1:c.2382G>C	XP_011517023.1:p.Val794=
XM_005252008.4:c.2382G>C	XP_005252065.1:p.Val794=
XM_006717121.3:c.2382G>C	XP_006717184.1:p.Val794=
XM_017014762.1:c.2793G>C	XP_016870251.1:p.Val931=
XM_017014763.1:c.2382G>C	XP_016870252.1:p.Val794=
NM_004560.4:c.2802G>C MANE Select	NP_004551.2:p.Val934=