Canonical Allele Identifier: CA465996401

Gene: ROR2

Linked Data

• gnomAD v4: 9-91726613-T-C
• MyVariant Identifiers: chr9:g.94488895T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726613T>C , CM000671.2:g.91726613T>C	GRCh38
NC_000009.11:g.94488895T>C , CM000671.1:g.94488895T>C	GRCh37
NC_000009.10:g.93528716T>C	NCBI36
NG_008089.1:g.228550A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1314A>G MANE Select	ENSP00000364860.3:p.Thr438=
ENST00000375708.3:c.1314A>G	ENSP00000364860.3:p.Thr438=
ENST00000375715.5:c.894A>G	ENSP00000364867.1:p.Thr298=
ENST00000550066.5:n.1782A>G
NM_004560.3:c.1314A>G	NP_004551.2:p.Thr438=
XM_005252008.3:c.894A>G	XP_005252065.1:p.Thr298=
XM_005252009.3:c.111A>G	XP_005252066.1:p.Thr37=
XM_006717121.2:c.894A>G	XP_006717184.1:p.Thr298=
XM_011518721.1:c.894A>G	XP_011517023.1:p.Thr298=
NM_001318204.1:c.1280A>G	NP_001305133.1:p.His427Arg
XM_005252008.4:c.894A>G	XP_005252065.1:p.Thr298=
XM_006717121.3:c.894A>G	XP_006717184.1:p.Thr298=
XM_017014762.1:c.1305A>G	XP_016870251.1:p.Thr435=
XM_017014763.1:c.894A>G	XP_016870252.1:p.Thr298=
XR_001746315.1:n.1523A>G
NM_004560.4:c.1314A>G MANE Select	NP_004551.2:p.Thr438=
NM_001318204.2:c.1280A>G	NP_001305133.1:p.His427Arg