Canonical Allele Identifier: CA373794351

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486356T>G (hg19) ; chr9:g.91724074T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724074T>G , CM000671.2:g.91724074T>G	GRCh38
NC_000009.11:g.94486356T>G , CM000671.1:g.94486356T>G	GRCh37
NC_000009.10:g.93526177T>G	NCBI36
NG_008089.1:g.231089A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2420A>C MANE Select	ENSP00000364860.3:p.Gln807Pro
ENST00000375708.3:c.2420A>C	ENSP00000364860.3:p.Gln807Pro
ENST00000375715.5:c.1920+80A>C	ENSP00000364867.1:n.1920+80A>C
ENST00000550066.5:n.2888A>C
NM_004560.3:c.2420A>C	NP_004551.2:p.Gln807Pro
XM_005252008.3:c.2000A>C	XP_005252065.1:p.Gln667Pro
XM_005252009.3:c.1217A>C	XP_005252066.1:p.Gln406Pro
XM_006717121.2:c.2000A>C	XP_006717184.1:p.Gln667Pro
XM_011518721.1:c.2000A>C	XP_011517023.1:p.Gln667Pro
XM_005252008.4:c.2000A>C	XP_005252065.1:p.Gln667Pro
XM_006717121.3:c.2000A>C	XP_006717184.1:p.Gln667Pro
XM_017014762.1:c.2411A>C	XP_016870251.1:p.Gln804Pro
XM_017014763.1:c.2000A>C	XP_016870252.1:p.Gln667Pro
NM_004560.4:c.2420A>C MANE Select	NP_004551.2:p.Gln807Pro