Canonical Allele Identifier: CA466339063

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486745G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724463G>A , CM000671.2:g.91724463G>A	GRCh38
NC_000009.11:g.94486745G>A , CM000671.1:g.94486745G>A	GRCh37
NC_000009.10:g.93526566G>A	NCBI36
NG_008089.1:g.230700C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2031C>T MANE Select	ENSP00000364860.3:p.Ser677=
ENST00000375708.3:c.2031C>T	ENSP00000364860.3:p.Ser677=
ENST00000375715.5:c.1611C>T	ENSP00000364867.1:p.Ser537=
ENST00000550066.5:n.2499C>T
NM_004560.3:c.2031C>T	NP_004551.2:p.Ser677=
XM_005252008.3:c.1611C>T	XP_005252065.1:p.Ser537=
XM_005252009.3:c.828C>T	XP_005252066.1:p.Ser276=
XM_006717121.2:c.1611C>T	XP_006717184.1:p.Ser537=
XM_011518721.1:c.1611C>T	XP_011517023.1:p.Ser537=
XM_005252008.4:c.1611C>T	XP_005252065.1:p.Ser537=
XM_006717121.3:c.1611C>T	XP_006717184.1:p.Ser537=
XM_017014762.1:c.2022C>T	XP_016870251.1:p.Ser674=
XM_017014763.1:c.1611C>T	XP_016870252.1:p.Ser537=
NM_004560.4:c.2031C>T MANE Select	NP_004551.2:p.Ser677=