Canonical Allele Identifier: CA373799421

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488894G>C (hg19) ; chr9:g.91726612G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726612G>C , CM000671.2:g.91726612G>C	GRCh38
NC_000009.11:g.94488894G>C , CM000671.1:g.94488894G>C	GRCh37
NC_000009.10:g.93528715G>C	NCBI36
NG_008089.1:g.228551C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1315C>G MANE Select	ENSP00000364860.3:p.Pro439Ala
ENST00000375708.3:c.1315C>G	ENSP00000364860.3:p.Pro439Ala
ENST00000375715.5:c.895C>G	ENSP00000364867.1:p.Pro299Ala
ENST00000550066.5:n.1783C>G
NM_004560.3:c.1315C>G	NP_004551.2:p.Pro439Ala
XM_005252008.3:c.895C>G	XP_005252065.1:p.Pro299Ala
XM_005252009.3:c.112C>G	XP_005252066.1:p.Pro38Ala
XM_006717121.2:c.895C>G	XP_006717184.1:p.Pro299Ala
XM_011518721.1:c.895C>G	XP_011517023.1:p.Pro299Ala
NM_001318204.1:c.1281C>G	NP_001305133.1:p.His427Gln
XM_005252008.4:c.895C>G	XP_005252065.1:p.Pro299Ala
XM_006717121.3:c.895C>G	XP_006717184.1:p.Pro299Ala
XM_017014762.1:c.1306C>G	XP_016870251.1:p.Pro436Ala
XM_017014763.1:c.895C>G	XP_016870252.1:p.Pro299Ala
XR_001746315.1:n.1524C>G
NM_004560.4:c.1315C>G MANE Select	NP_004551.2:p.Pro439Ala
NM_001318204.2:c.1281C>G	NP_001305133.1:p.His427Gln