Canonical Allele Identifier: CA466359436

Gene: ROR2

Linked Data

• gnomAD v4: 9-91757432-C-G
• MyVariant Identifiers: chr9:g.94519714C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757432C>G , CM000671.2:g.91757432C>G	GRCh38
NC_000009.11:g.94519714C>G , CM000671.1:g.94519714C>G	GRCh37
NC_000009.10:g.93559535C>G	NCBI36
NG_008089.1:g.197731G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.303G>C MANE Select	ENSP00000364860.3:p.Pro101=
ENST00000375708.3:c.303G>C	ENSP00000364860.3:p.Pro101=
ENST00000375715.5:c.-118G>C	ENSP00000364867.1:n.-118G>C
ENST00000495386.5:n.566G>C
ENST00000548585.2:n.169G>C
ENST00000550066.5:n.771G>C
NM_004560.3:c.303G>C	NP_004551.2:p.Pro101=
XM_005252008.3:c.-118G>C	XP_005252065.1:n.-118G>C
XM_006717121.2:c.-118G>C	XP_006717184.1:n.-118G>C
XM_011518721.1:c.-118G>C	XP_011517023.1:n.-118G>C
NM_001318204.1:c.303G>C	NP_001305133.1:p.Pro101=
XM_005252008.4:c.-118G>C	XP_005252065.1:n.-118G>C
XM_006717121.3:c.-118G>C	XP_006717184.1:n.-118G>C
XM_017014762.1:c.294G>C	XP_016870251.1:p.Pro98=
XM_017014763.1:c.-118G>C	XP_016870252.1:n.-118G>C
XR_001746315.1:n.546G>C
NM_004560.4:c.303G>C MANE Select	NP_004551.2:p.Pro101=
NM_001318204.2:c.303G>C	NP_001305133.1:p.Pro101=