Canonical Allele Identifier: CA465996357

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488885G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726603G>T , CM000671.2:g.91726603G>T	GRCh38
NC_000009.11:g.94488885G>T , CM000671.1:g.94488885G>T	GRCh37
NC_000009.10:g.93528706G>T	NCBI36
NG_008089.1:g.228560C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1324C>A MANE Select	ENSP00000364860.3:p.Arg442=
ENST00000375708.3:c.1324C>A	ENSP00000364860.3:p.Arg442=
ENST00000375715.5:c.904C>A	ENSP00000364867.1:p.Arg302=
ENST00000550066.5:n.1792C>A
NM_004560.3:c.1324C>A	NP_004551.2:p.Arg442=
XM_005252008.3:c.904C>A	XP_005252065.1:p.Arg302=
XM_005252009.3:c.121C>A	XP_005252066.1:p.Arg41=
XM_006717121.2:c.904C>A	XP_006717184.1:p.Arg302=
XM_011518721.1:c.904C>A	XP_011517023.1:p.Arg302=
NM_001318204.1:c.1290C>A	NP_001305133.1:p.Gly430=
XM_005252008.4:c.904C>A	XP_005252065.1:p.Arg302=
XM_006717121.3:c.904C>A	XP_006717184.1:p.Arg302=
XM_017014762.1:c.1315C>A	XP_016870251.1:p.Arg439=
XM_017014763.1:c.904C>A	XP_016870252.1:p.Arg302=
XR_001746315.1:n.1533C>A
NM_004560.4:c.1324C>A MANE Select	NP_004551.2:p.Arg442=
NM_001318204.2:c.1290C>A	NP_001305133.1:p.Gly430=