Canonical Allele Identifier: CA466359595

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519810G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757528G>A , CM000671.2:g.91757528G>A	GRCh38
NC_000009.11:g.94519810G>A , CM000671.1:g.94519810G>A	GRCh37
NC_000009.10:g.93559631G>A	NCBI36
NG_008089.1:g.197635C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.207C>T MANE Select	ENSP00000364860.3:p.Asn69=
ENST00000375708.3:c.207C>T	ENSP00000364860.3:p.Asn69=
ENST00000375715.5:c.-214C>T	ENSP00000364867.1:n.-214C>T
ENST00000495386.5:n.470C>T
ENST00000546883.1:n.409C>T
ENST00000548585.2:n.73C>T
ENST00000550066.5:n.675C>T
NM_004560.3:c.207C>T	NP_004551.2:p.Asn69=
XM_005252008.3:c.-214C>T	XP_005252065.1:n.-214C>T
XM_006717121.2:c.-214C>T	XP_006717184.1:n.-214C>T
XM_011518721.1:c.-214C>T	XP_011517023.1:n.-214C>T
NM_001318204.1:c.207C>T	NP_001305133.1:p.Asn69=
XM_005252008.4:c.-214C>T	XP_005252065.1:n.-214C>T
XM_006717121.3:c.-214C>T	XP_006717184.1:n.-214C>T
XM_017014762.1:c.198C>T	XP_016870251.1:p.Asn66=
XM_017014763.1:c.-214C>T	XP_016870252.1:n.-214C>T
XR_001746315.1:n.450C>T
NM_004560.4:c.207C>T MANE Select	NP_004551.2:p.Asn69=
NM_001318204.2:c.207C>T	NP_001305133.1:p.Asn69=