Canonical Allele Identifier: CA203749

Gene: ROR2

Linked Data

• ClinVar Variation Id: 199097
• ClinVar RCV Id: RCV000180605 ; RCV000357547 ; RCV000305022 ; RCV001689719
• dbSNP Id: rs2230578
• ExAC: 9:94485928 C / T
• gnomAD v2: 9-94485928-C-T
• gnomAD v3: 9-91723646-C-T
• gnomAD v4: 9-91723646-C-T
• MyVariant Identifiers: chr9:g.94485928C>T (hg19) ; chr9:g.91723646C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723646C>T , CM000671.2:g.91723646C>T	GRCh38
NC_000009.11:g.94485928C>T , CM000671.1:g.94485928C>T	GRCh37
NC_000009.10:g.93525749C>T	NCBI36
NG_008089.1:g.231517G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*16G>A MANE Select	ENSP00000364860.3:n.*16G>A
ENST00000375708.3:c.*16G>A	ENSP00000364860.3:n.*16G>A
ENST00000375715.5:c.1920+508G>A	ENSP00000364867.1:n.1920+508G>A
ENST00000550066.5:n.3316G>A
NM_004560.3:c.*16G>A	NP_004551.2:n.*16G>A
XM_005252008.3:c.*16G>A	XP_005252065.1:n.*16G>A
XM_005252009.3:c.*16G>A	XP_005252066.1:n.*16G>A
XM_006717121.2:c.*16G>A	XP_006717184.1:n.*16G>A
XM_011518721.1:c.*16G>A	XP_011517023.1:n.*16G>A
XM_005252008.4:c.*16G>A	XP_005252065.1:n.*16G>A
XM_006717121.3:c.*16G>A	XP_006717184.1:n.*16G>A
XM_017014762.1:c.*16G>A	XP_016870251.1:n.*16G>A
XM_017014763.1:c.*16G>A	XP_016870252.1:n.*16G>A
NM_004560.4:c.*16G>A MANE Select	NP_004551.2:n.*16G>A