Canonical Allele Identifier: CA373793882

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486230T>G (hg19) ; chr9:g.91723948T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723948T>G , CM000671.2:g.91723948T>G	GRCh38
NC_000009.11:g.94486230T>G , CM000671.1:g.94486230T>G	GRCh37
NC_000009.10:g.93526051T>G	NCBI36
NG_008089.1:g.231215A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2546A>C MANE Select	ENSP00000364860.3:p.Gln849Pro
ENST00000375708.3:c.2546A>C	ENSP00000364860.3:p.Gln849Pro
ENST00000375715.5:c.1920+206A>C	ENSP00000364867.1:n.1920+206A>C
ENST00000550066.5:n.3014A>C
NM_004560.3:c.2546A>C	NP_004551.2:p.Gln849Pro
XM_005252008.3:c.2126A>C	XP_005252065.1:p.Gln709Pro
XM_005252009.3:c.1343A>C	XP_005252066.1:p.Gln448Pro
XM_006717121.2:c.2126A>C	XP_006717184.1:p.Gln709Pro
XM_011518721.1:c.2126A>C	XP_011517023.1:p.Gln709Pro
XM_005252008.4:c.2126A>C	XP_005252065.1:p.Gln709Pro
XM_006717121.3:c.2126A>C	XP_006717184.1:p.Gln709Pro
XM_017014762.1:c.2537A>C	XP_016870251.1:p.Gln846Pro
XM_017014763.1:c.2126A>C	XP_016870252.1:p.Gln709Pro
NM_004560.4:c.2546A>C MANE Select	NP_004551.2:p.Gln849Pro