Canonical Allele Identifier: CA466359498

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519750T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757468T>A , CM000671.2:g.91757468T>A	GRCh38
NC_000009.11:g.94519750T>A , CM000671.1:g.94519750T>A	GRCh37
NC_000009.10:g.93559571T>A	NCBI36
NG_008089.1:g.197695A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.267A>T MANE Select	ENSP00000364860.3:p.Pro89=
ENST00000375708.3:c.267A>T	ENSP00000364860.3:p.Pro89=
ENST00000375715.5:c.-154A>T	ENSP00000364867.1:n.-154A>T
ENST00000495386.5:n.530A>T
ENST00000546883.1:n.469A>T
ENST00000548585.2:n.133A>T
ENST00000550066.5:n.735A>T
NM_004560.3:c.267A>T	NP_004551.2:p.Pro89=
XM_005252008.3:c.-154A>T	XP_005252065.1:n.-154A>T
XM_006717121.2:c.-154A>T	XP_006717184.1:n.-154A>T
XM_011518721.1:c.-154A>T	XP_011517023.1:n.-154A>T
NM_001318204.1:c.267A>T	NP_001305133.1:p.Pro89=
XM_005252008.4:c.-154A>T	XP_005252065.1:n.-154A>T
XM_006717121.3:c.-154A>T	XP_006717184.1:n.-154A>T
XM_017014762.1:c.258A>T	XP_016870251.1:p.Pro86=
XM_017014763.1:c.-154A>T	XP_016870252.1:n.-154A>T
XR_001746315.1:n.510A>T
NM_004560.4:c.267A>T MANE Select	NP_004551.2:p.Pro89=
NM_001318204.2:c.267A>T	NP_001305133.1:p.Pro89=