Canonical Allele Identifier: CA2599989610

Gene: ROR2

Linked Data

• dbSNP Id: rs950947484
• gnomAD v3: 9-91723561-G-C
• gnomAD v4: 9-91723561-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723561G>C , CM000671.2:g.91723561G>C	GRCh38
NC_000009.11:g.94485843G>C , CM000671.1:g.94485843G>C	GRCh37
NC_000009.10:g.93525664G>C	NCBI36
NG_008089.1:g.231602C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*101C>G MANE Select	ENSP00000364860.3:n.*101C>G
ENST00000375708.3:c.*101C>G	ENSP00000364860.3:n.*101C>G
ENST00000375715.5:c.1920+593C>G	ENSP00000364867.1:n.1920+593C>G
ENST00000550066.5:n.3401C>G
NM_004560.3:c.*101C>G	NP_004551.2:n.*101C>G
XM_005252008.3:c.*101C>G	XP_005252065.1:n.*101C>G
XM_005252009.3:c.*101C>G	XP_005252066.1:n.*101C>G
XM_006717121.2:c.*101C>G	XP_006717184.1:n.*101C>G
XM_011518721.1:c.*101C>G	XP_011517023.1:n.*101C>G
XM_005252008.4:c.*101C>G	XP_005252065.1:n.*101C>G
XM_006717121.3:c.*101C>G	XP_006717184.1:n.*101C>G
XM_017014762.1:c.*101C>G	XP_016870251.1:n.*101C>G
XM_017014763.1:c.*101C>G	XP_016870252.1:n.*101C>G
NM_004560.4:c.*101C>G MANE Select	NP_004551.2:n.*101C>G