Canonical Allele Identifier: CA373797300

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486921G>C (hg19) ; chr9:g.91724639G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724639G>C , CM000671.2:g.91724639G>C	GRCh38
NC_000009.11:g.94486921G>C , CM000671.1:g.94486921G>C	GRCh37
NC_000009.10:g.93526742G>C	NCBI36
NG_008089.1:g.230524C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1855C>G MANE Select	ENSP00000364860.3:p.Arg619Gly
ENST00000375708.3:c.1855C>G	ENSP00000364860.3:p.Arg619Gly
ENST00000375715.5:c.1435C>G	ENSP00000364867.1:p.Arg479Gly
ENST00000550066.5:n.2323C>G
NM_004560.3:c.1855C>G	NP_004551.2:p.Arg619Gly
XM_005252008.3:c.1435C>G	XP_005252065.1:p.Arg479Gly
XM_005252009.3:c.652C>G	XP_005252066.1:p.Arg218Gly
XM_006717121.2:c.1435C>G	XP_006717184.1:p.Arg479Gly
XM_011518721.1:c.1435C>G	XP_011517023.1:p.Arg479Gly
XM_005252008.4:c.1435C>G	XP_005252065.1:p.Arg479Gly
XM_006717121.3:c.1435C>G	XP_006717184.1:p.Arg479Gly
XM_017014762.1:c.1846C>G	XP_016870251.1:p.Arg616Gly
XM_017014763.1:c.1435C>G	XP_016870252.1:p.Arg479Gly
NM_004560.4:c.1855C>G MANE Select	NP_004551.2:p.Arg619Gly