Canonical Allele Identifier: CA466359517

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519759T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757477T>G , CM000671.2:g.91757477T>G	GRCh38
NC_000009.11:g.94519759T>G , CM000671.1:g.94519759T>G	GRCh37
NC_000009.10:g.93559580T>G	NCBI36
NG_008089.1:g.197686A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.258A>C MANE Select	ENSP00000364860.3:p.Ala86=
ENST00000375708.3:c.258A>C	ENSP00000364860.3:p.Ala86=
ENST00000375715.5:c.-163A>C	ENSP00000364867.1:n.-163A>C
ENST00000495386.5:n.521A>C
ENST00000546883.1:n.460A>C
ENST00000548585.2:n.124A>C
ENST00000550066.5:n.726A>C
NM_004560.3:c.258A>C	NP_004551.2:p.Ala86=
XM_005252008.3:c.-163A>C	XP_005252065.1:n.-163A>C
XM_006717121.2:c.-163A>C	XP_006717184.1:n.-163A>C
XM_011518721.1:c.-163A>C	XP_011517023.1:n.-163A>C
NM_001318204.1:c.258A>C	NP_001305133.1:p.Ala86=
XM_005252008.4:c.-163A>C	XP_005252065.1:n.-163A>C
XM_006717121.3:c.-163A>C	XP_006717184.1:n.-163A>C
XM_017014762.1:c.249A>C	XP_016870251.1:p.Ala83=
XM_017014763.1:c.-163A>C	XP_016870252.1:n.-163A>C
XR_001746315.1:n.501A>C
NM_004560.4:c.258A>C MANE Select	NP_004551.2:p.Ala86=
NM_001318204.2:c.258A>C	NP_001305133.1:p.Ala86=