Canonical Allele Identifier: CA373799239

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488822C>G (hg19) ; chr9:g.91726540C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726540C>G , CM000671.2:g.91726540C>G	GRCh38
NC_000009.11:g.94488822C>G , CM000671.1:g.94488822C>G	GRCh37
NC_000009.10:g.93528643C>G	NCBI36
NG_008089.1:g.228623G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1386+1G>C MANE Select	ENSP00000364860.3:n.1386+1G>C
ENST00000375708.3:c.1386+1G>C	ENSP00000364860.3:n.1386+1G>C
ENST00000375715.5:c.966+1G>C	ENSP00000364867.1:n.966+1G>C
ENST00000550066.5:n.1854+1G>C
NM_004560.3:c.1386+1G>C	NP_004551.2:n.1386+1G>C
XM_005252008.3:c.966+1G>C	XP_005252065.1:n.966+1G>C
XM_005252009.3:c.183+1G>C	XP_005252066.1:n.183+1G>C
XM_006717121.2:c.966+1G>C	XP_006717184.1:n.966+1G>C
XM_011518721.1:c.966+1G>C	XP_011517023.1:n.966+1G>C
NM_001318204.1:c.*54G>C	NP_001305133.1:n.*54G>C
XM_005252008.4:c.966+1G>C	XP_005252065.1:n.966+1G>C
XM_006717121.3:c.966+1G>C	XP_006717184.1:n.966+1G>C
XM_017014762.1:c.1377+1G>C	XP_016870251.1:n.1377+1G>C
XM_017014763.1:c.966+1G>C	XP_016870252.1:n.966+1G>C
XR_001746315.1:n.1595+1G>C
NM_004560.4:c.1386+1G>C MANE Select	NP_004551.2:n.1386+1G>C
NM_001318204.2:c.*54G>C	NP_001305133.1:n.*54G>C