Canonical Allele Identifier: CA466334551

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486223C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723941C>A , CM000671.2:g.91723941C>A	GRCh38
NC_000009.11:g.94486223C>A , CM000671.1:g.94486223C>A	GRCh37
NC_000009.10:g.93526044C>A	NCBI36
NG_008089.1:g.231222G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2553G>T MANE Select	ENSP00000364860.3:p.Val851=
ENST00000375708.3:c.2553G>T	ENSP00000364860.3:p.Val851=
ENST00000375715.5:c.1920+213G>T	ENSP00000364867.1:n.1920+213G>T
ENST00000550066.5:n.3021G>T
NM_004560.3:c.2553G>T	NP_004551.2:p.Val851=
XM_005252008.3:c.2133G>T	XP_005252065.1:p.Val711=
XM_005252009.3:c.1350G>T	XP_005252066.1:p.Val450=
XM_006717121.2:c.2133G>T	XP_006717184.1:p.Val711=
XM_011518721.1:c.2133G>T	XP_011517023.1:p.Val711=
XM_005252008.4:c.2133G>T	XP_005252065.1:p.Val711=
XM_006717121.3:c.2133G>T	XP_006717184.1:p.Val711=
XM_017014762.1:c.2544G>T	XP_016870251.1:p.Val848=
XM_017014763.1:c.2133G>T	XP_016870252.1:p.Val711=
NM_004560.4:c.2553G>T MANE Select	NP_004551.2:p.Val851=