Canonical Allele Identifier: CA5120288

Gene: ROR2

Linked Data

• ClinVar Variation Id: 914738
• ClinVar RCV Id: RCV001169057 ; RCV001169058
• dbSNP Id: rs759105926
• ExAC: 9:94485898 G / A
• gnomAD v2: 9-94485898-G-A
• gnomAD v3: 9-91723616-G-A
• gnomAD v4: 9-91723616-G-A
• MyVariant Identifiers: chr9:g.94485898G>A (hg19) ; chr9:g.91723616G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723616G>A , CM000671.2:g.91723616G>A	GRCh38
NC_000009.11:g.94485898G>A , CM000671.1:g.94485898G>A	GRCh37
NC_000009.10:g.93525719G>A	NCBI36
NG_008089.1:g.231547C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*46C>T MANE Select	ENSP00000364860.3:n.*46C>T
ENST00000375708.3:c.*46C>T	ENSP00000364860.3:n.*46C>T
ENST00000375715.5:c.1920+538C>T	ENSP00000364867.1:n.1920+538C>T
ENST00000550066.5:n.3346C>T
NM_004560.3:c.*46C>T	NP_004551.2:n.*46C>T
XM_005252008.3:c.*46C>T	XP_005252065.1:n.*46C>T
XM_005252009.3:c.*46C>T	XP_005252066.1:n.*46C>T
XM_006717121.2:c.*46C>T	XP_006717184.1:n.*46C>T
XM_011518721.1:c.*46C>T	XP_011517023.1:n.*46C>T
XM_005252008.4:c.*46C>T	XP_005252065.1:n.*46C>T
XM_006717121.3:c.*46C>T	XP_006717184.1:n.*46C>T
XM_017014762.1:c.*46C>T	XP_016870251.1:n.*46C>T
XM_017014763.1:c.*46C>T	XP_016870252.1:n.*46C>T
NM_004560.4:c.*46C>T MANE Select	NP_004551.2:n.*46C>T