Canonical Allele Identifier: CA466359475

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519735C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757453C>T , CM000671.2:g.91757453C>T	GRCh38
NC_000009.11:g.94519735C>T , CM000671.1:g.94519735C>T	GRCh37
NC_000009.10:g.93559556C>T	NCBI36
NG_008089.1:g.197710G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.282G>A MANE Select	ENSP00000364860.3:p.Arg94=
ENST00000375708.3:c.282G>A	ENSP00000364860.3:p.Arg94=
ENST00000375715.5:c.-139G>A	ENSP00000364867.1:n.-139G>A
ENST00000495386.5:n.545G>A
ENST00000546883.1:n.484G>A
ENST00000548585.2:n.148G>A
ENST00000550066.5:n.750G>A
NM_004560.3:c.282G>A	NP_004551.2:p.Arg94=
XM_005252008.3:c.-139G>A	XP_005252065.1:n.-139G>A
XM_006717121.2:c.-139G>A	XP_006717184.1:n.-139G>A
XM_011518721.1:c.-139G>A	XP_011517023.1:n.-139G>A
NM_001318204.1:c.282G>A	NP_001305133.1:p.Arg94=
XM_005252008.4:c.-139G>A	XP_005252065.1:n.-139G>A
XM_006717121.3:c.-139G>A	XP_006717184.1:n.-139G>A
XM_017014762.1:c.273G>A	XP_016870251.1:p.Arg91=
XM_017014763.1:c.-139G>A	XP_016870252.1:n.-139G>A
XR_001746315.1:n.525G>A
NM_004560.4:c.282G>A MANE Select	NP_004551.2:p.Arg94=
NM_001318204.2:c.282G>A	NP_001305133.1:p.Arg94=