Canonical Allele Identifier: CA373796804

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486813G>C (hg19) ; chr9:g.91724531G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724531G>C , CM000671.2:g.91724531G>C	GRCh38
NC_000009.11:g.94486813G>C , CM000671.1:g.94486813G>C	GRCh37
NC_000009.10:g.93526634G>C	NCBI36
NG_008089.1:g.230632C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1963C>G MANE Select	ENSP00000364860.3:p.Pro655Ala
ENST00000375708.3:c.1963C>G	ENSP00000364860.3:p.Pro655Ala
ENST00000375715.5:c.1543C>G	ENSP00000364867.1:p.Pro515Ala
ENST00000550066.5:n.2431C>G
NM_004560.3:c.1963C>G	NP_004551.2:p.Pro655Ala
XM_005252008.3:c.1543C>G	XP_005252065.1:p.Pro515Ala
XM_005252009.3:c.760C>G	XP_005252066.1:p.Pro254Ala
XM_006717121.2:c.1543C>G	XP_006717184.1:p.Pro515Ala
XM_011518721.1:c.1543C>G	XP_011517023.1:p.Pro515Ala
XM_005252008.4:c.1543C>G	XP_005252065.1:p.Pro515Ala
XM_006717121.3:c.1543C>G	XP_006717184.1:p.Pro515Ala
XM_017014762.1:c.1954C>G	XP_016870251.1:p.Pro652Ala
XM_017014763.1:c.1543C>G	XP_016870252.1:p.Pro515Ala
NM_004560.4:c.1963C>G MANE Select	NP_004551.2:p.Pro655Ala