Canonical Allele Identifier: CA373793878

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486229C>G (hg19) ; chr9:g.91723947C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723947C>G , CM000671.2:g.91723947C>G	GRCh38
NC_000009.11:g.94486229C>G , CM000671.1:g.94486229C>G	GRCh37
NC_000009.10:g.93526050C>G	NCBI36
NG_008089.1:g.231216G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2547G>C MANE Select	ENSP00000364860.3:p.Gln849His
ENST00000375708.3:c.2547G>C	ENSP00000364860.3:p.Gln849His
ENST00000375715.5:c.1920+207G>C	ENSP00000364867.1:n.1920+207G>C
ENST00000550066.5:n.3015G>C
NM_004560.3:c.2547G>C	NP_004551.2:p.Gln849His
XM_005252008.3:c.2127G>C	XP_005252065.1:p.Gln709His
XM_005252009.3:c.1344G>C	XP_005252066.1:p.Gln448His
XM_006717121.2:c.2127G>C	XP_006717184.1:p.Gln709His
XM_011518721.1:c.2127G>C	XP_011517023.1:p.Gln709His
XM_005252008.4:c.2127G>C	XP_005252065.1:p.Gln709His
XM_006717121.3:c.2127G>C	XP_006717184.1:p.Gln709His
XM_017014762.1:c.2538G>C	XP_016870251.1:p.Gln846His
XM_017014763.1:c.2127G>C	XP_016870252.1:p.Gln709His
NM_004560.4:c.2547G>C MANE Select	NP_004551.2:p.Gln849His