Canonical Allele Identifier: CA466359023

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519561C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757279C>G , CM000671.2:g.91757279C>G	GRCh38
NC_000009.11:g.94519561C>G , CM000671.1:g.94519561C>G	GRCh37
NC_000009.10:g.93559382C>G	NCBI36
NG_008089.1:g.197884G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.456G>C MANE Select	ENSP00000364860.3:p.Val152=
ENST00000375708.3:c.456G>C	ENSP00000364860.3:p.Val152=
ENST00000375715.5:c.36G>C	ENSP00000364867.1:p.Val12=
ENST00000548585.2:n.172+150G>C
ENST00000550066.5:n.924G>C
NM_004560.3:c.456G>C	NP_004551.2:p.Val152=
XM_005252008.3:c.36G>C	XP_005252065.1:p.Val12=
XM_006717121.2:c.36G>C	XP_006717184.1:p.Val12=
XM_011518721.1:c.36G>C	XP_011517023.1:p.Val12=
NM_001318204.1:c.456G>C	NP_001305133.1:p.Val152=
XM_005252008.4:c.36G>C	XP_005252065.1:p.Val12=
XM_006717121.3:c.36G>C	XP_006717184.1:p.Val12=
XM_017014762.1:c.447G>C	XP_016870251.1:p.Val149=
XM_017014763.1:c.36G>C	XP_016870252.1:p.Val12=
XR_001746315.1:n.699G>C
NM_004560.4:c.456G>C MANE Select	NP_004551.2:p.Val152=
NM_001318204.2:c.456G>C	NP_001305133.1:p.Val152=