Canonical Allele Identifier: CA373796779

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486807G>T (hg19) ; chr9:g.91724525G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724525G>T , CM000671.2:g.91724525G>T	GRCh38
NC_000009.11:g.94486807G>T , CM000671.1:g.94486807G>T	GRCh37
NC_000009.10:g.93526628G>T	NCBI36
NG_008089.1:g.230638C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1969C>A MANE Select	ENSP00000364860.3:p.Arg657Ser
ENST00000375708.3:c.1969C>A	ENSP00000364860.3:p.Arg657Ser
ENST00000375715.5:c.1549C>A	ENSP00000364867.1:p.Arg517Ser
ENST00000550066.5:n.2437C>A
NM_004560.3:c.1969C>A	NP_004551.2:p.Arg657Ser
XM_005252008.3:c.1549C>A	XP_005252065.1:p.Arg517Ser
XM_005252009.3:c.766C>A	XP_005252066.1:p.Arg256Ser
XM_006717121.2:c.1549C>A	XP_006717184.1:p.Arg517Ser
XM_011518721.1:c.1549C>A	XP_011517023.1:p.Arg517Ser
XM_005252008.4:c.1549C>A	XP_005252065.1:p.Arg517Ser
XM_006717121.3:c.1549C>A	XP_006717184.1:p.Arg517Ser
XM_017014762.1:c.1960C>A	XP_016870251.1:p.Arg654Ser
XM_017014763.1:c.1549C>A	XP_016870252.1:p.Arg517Ser
NM_004560.4:c.1969C>A MANE Select	NP_004551.2:p.Arg657Ser