Canonical Allele Identifier: CA10627662

Gene: ROR2

Linked Data

• ClinVar Variation Id: 367508
• ClinVar RCV Id: RCV000302280 ; RCV000401531
• dbSNP Id: rs1057515681
• MyVariant Identifiers: chr9:g.94488975T>C (hg19) ; chr9:g.91726693T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726693T>C , CM000671.2:g.91726693T>C	GRCh38
NC_000009.11:g.94488975T>C , CM000671.1:g.94488975T>C	GRCh37
NC_000009.10:g.93528796T>C	NCBI36
NG_008089.1:g.228470A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1234A>G MANE Select	ENSP00000364860.3:p.Ile412Val
ENST00000375708.3:c.1234A>G	ENSP00000364860.3:p.Ile412Val
ENST00000375715.5:c.814A>G	ENSP00000364867.1:p.Ile272Val
ENST00000550066.5:n.1702A>G
NM_004560.3:c.1234A>G	NP_004551.2:p.Ile412Val
XM_005252008.3:c.814A>G	XP_005252065.1:p.Ile272Val
XM_005252009.3:c.31A>G	XP_005252066.1:p.Ile11Val
XM_006717121.2:c.814A>G	XP_006717184.1:p.Ile272Val
XM_011518721.1:c.814A>G	XP_011517023.1:p.Ile272Val
NM_001318204.1:c.1200A>G	NP_001305133.1:p.Ala400=
XM_005252008.4:c.814A>G	XP_005252065.1:p.Ile272Val
XM_006717121.3:c.814A>G	XP_006717184.1:p.Ile272Val
XM_017014762.1:c.1225A>G	XP_016870251.1:p.Ile409Val
XM_017014763.1:c.814A>G	XP_016870252.1:p.Ile272Val
XR_001746315.1:n.1443A>G
NM_004560.4:c.1234A>G MANE Select	NP_004551.2:p.Ile412Val
NM_001318204.2:c.1200A>G	NP_001305133.1:p.Ala400=