Canonical Allele Identifier: CA465995379

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94485959G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723677G>C , CM000671.2:g.91723677G>C	GRCh38
NC_000009.11:g.94485959G>C , CM000671.1:g.94485959G>C	GRCh37
NC_000009.10:g.93525780G>C	NCBI36
NG_008089.1:g.231486C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2817C>G MANE Select	ENSP00000364860.3:p.Val939=
ENST00000375708.3:c.2817C>G	ENSP00000364860.3:p.Val939=
ENST00000375715.5:c.1920+477C>G	ENSP00000364867.1:n.1920+477C>G
ENST00000550066.5:n.3285C>G
NM_004560.3:c.2817C>G	NP_004551.2:p.Val939=
XM_005252008.3:c.2397C>G	XP_005252065.1:p.Val799=
XM_005252009.3:c.1614C>G	XP_005252066.1:p.Val538=
XM_006717121.2:c.2397C>G	XP_006717184.1:p.Val799=
XM_011518721.1:c.2397C>G	XP_011517023.1:p.Val799=
XM_005252008.4:c.2397C>G	XP_005252065.1:p.Val799=
XM_006717121.3:c.2397C>G	XP_006717184.1:p.Val799=
XM_017014762.1:c.2808C>G	XP_016870251.1:p.Val936=
XM_017014763.1:c.2397C>G	XP_016870252.1:p.Val799=
NM_004560.4:c.2817C>G MANE Select	NP_004551.2:p.Val939=