Canonical Allele Identifier: CA5121036

Gene: ROR2

Linked Data

• ClinVar Variation Id: 1485199
• ClinVar RCV Id: RCV002008480 ; RCV002492248 ; RCV003170382
• dbSNP Id: rs745695427
• ExAC: 9:94519560 G / A
• gnomAD v2: 9-94519560-G-A
• gnomAD v3: 9-91757278-G-A
• gnomAD v4: 9-91757278-G-A
• COSMIC: COSM1472286
• MyVariant Identifiers: chr9:g.94519560G>A (hg19) ; chr9:g.91757278G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757278G>A , CM000671.2:g.91757278G>A	GRCh38
NC_000009.11:g.94519560G>A , CM000671.1:g.94519560G>A	GRCh37
NC_000009.10:g.93559381G>A	NCBI36
NG_008089.1:g.197885C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.457C>T MANE Select	ENSP00000364860.3:p.Arg153Trp
ENST00000375708.3:c.457C>T	ENSP00000364860.3:p.Arg153Trp
ENST00000375715.5:c.37C>T	ENSP00000364867.1:p.Arg13Trp
ENST00000548585.2:n.172+151C>T
ENST00000550066.5:n.925C>T
NM_004560.3:c.457C>T	NP_004551.2:p.Arg153Trp
XM_005252008.3:c.37C>T	XP_005252065.1:p.Arg13Trp
XM_006717121.2:c.37C>T	XP_006717184.1:p.Arg13Trp
XM_011518721.1:c.37C>T	XP_011517023.1:p.Arg13Trp
NM_001318204.1:c.457C>T	NP_001305133.1:p.Arg153Trp
XM_005252008.4:c.37C>T	XP_005252065.1:p.Arg13Trp
XM_006717121.3:c.37C>T	XP_006717184.1:p.Arg13Trp
XM_017014762.1:c.448C>T	XP_016870251.1:p.Arg150Trp
XM_017014763.1:c.37C>T	XP_016870252.1:p.Arg13Trp
XR_001746315.1:n.700C>T
NM_004560.4:c.457C>T MANE Select	NP_004551.2:p.Arg153Trp
NM_001318204.2:c.457C>T	NP_001305133.1:p.Arg153Trp