Canonical Allele Identifier: CA465996346

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488883T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726601T>A , CM000671.2:g.91726601T>A	GRCh38
NC_000009.11:g.94488883T>A , CM000671.1:g.94488883T>A	GRCh37
NC_000009.10:g.93528704T>A	NCBI36
NG_008089.1:g.228562A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1326A>T MANE Select	ENSP00000364860.3:p.Arg442=
ENST00000375708.3:c.1326A>T	ENSP00000364860.3:p.Arg442=
ENST00000375715.5:c.906A>T	ENSP00000364867.1:p.Arg302=
ENST00000550066.5:n.1794A>T
NM_004560.3:c.1326A>T	NP_004551.2:p.Arg442=
XM_005252008.3:c.906A>T	XP_005252065.1:p.Arg302=
XM_005252009.3:c.123A>T	XP_005252066.1:p.Arg41=
XM_006717121.2:c.906A>T	XP_006717184.1:p.Arg302=
XM_011518721.1:c.906A>T	XP_011517023.1:p.Arg302=
NM_001318204.1:c.1292A>T	NP_001305133.1:p.Asp431Val
XM_005252008.4:c.906A>T	XP_005252065.1:p.Arg302=
XM_006717121.3:c.906A>T	XP_006717184.1:p.Arg302=
XM_017014762.1:c.1317A>T	XP_016870251.1:p.Arg439=
XM_017014763.1:c.906A>T	XP_016870252.1:p.Arg302=
XR_001746315.1:n.1535A>T
NM_004560.4:c.1326A>T MANE Select	NP_004551.2:p.Arg442=
NM_001318204.2:c.1292A>T	NP_001305133.1:p.Asp431Val