Canonical Allele Identifier: CA1863925394

Gene: ROR2

Linked Data

• dbSNP Id: rs1837039941
• gnomAD v4: 9-91726521-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726521A>G , CM000671.2:g.91726521A>G	GRCh38
NC_000009.11:g.94488803A>G , CM000671.1:g.94488803A>G	GRCh37
NC_000009.10:g.93528624A>G	NCBI36
NG_008089.1:g.228642T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1386+20T>C MANE Select	ENSP00000364860.3:n.1386+20T>C
ENST00000375708.3:c.1386+20T>C	ENSP00000364860.3:n.1386+20T>C
ENST00000375715.5:c.966+20T>C	ENSP00000364867.1:n.966+20T>C
ENST00000550066.5:n.1854+20T>C
NM_004560.3:c.1386+20T>C	NP_004551.2:n.1386+20T>C
XM_005252008.3:c.966+20T>C	XP_005252065.1:n.966+20T>C
XM_005252009.3:c.183+20T>C	XP_005252066.1:n.183+20T>C
XM_006717121.2:c.966+20T>C	XP_006717184.1:n.966+20T>C
XM_011518721.1:c.966+20T>C	XP_011517023.1:n.966+20T>C
NM_001318204.1:c.*73T>C	NP_001305133.1:n.*73T>C
XM_005252008.4:c.966+20T>C	XP_005252065.1:n.966+20T>C
XM_006717121.3:c.966+20T>C	XP_006717184.1:n.966+20T>C
XM_017014762.1:c.1377+20T>C	XP_016870251.1:n.1377+20T>C
XM_017014763.1:c.966+20T>C	XP_016870252.1:n.966+20T>C
XR_001746315.1:n.1595+20T>C
NM_004560.4:c.1386+20T>C MANE Select	NP_004551.2:n.1386+20T>C
NM_001318204.2:c.*73T>C	NP_001305133.1:n.*73T>C