Canonical Allele Identifier: CA373794417

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486373G>C (hg19) ; chr9:g.91724091G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724091G>C , CM000671.2:g.91724091G>C	GRCh38
NC_000009.11:g.94486373G>C , CM000671.1:g.94486373G>C	GRCh37
NC_000009.10:g.93526194G>C	NCBI36
NG_008089.1:g.231072C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2403C>G MANE Select	ENSP00000364860.3:p.Phe801Leu
ENST00000375708.3:c.2403C>G	ENSP00000364860.3:p.Phe801Leu
ENST00000375715.5:c.1920+63C>G	ENSP00000364867.1:n.1920+63C>G
ENST00000550066.5:n.2871C>G
NM_004560.3:c.2403C>G	NP_004551.2:p.Phe801Leu
XM_005252008.3:c.1983C>G	XP_005252065.1:p.Phe661Leu
XM_005252009.3:c.1200C>G	XP_005252066.1:p.Phe400Leu
XM_006717121.2:c.1983C>G	XP_006717184.1:p.Phe661Leu
XM_011518721.1:c.1983C>G	XP_011517023.1:p.Phe661Leu
XM_005252008.4:c.1983C>G	XP_005252065.1:p.Phe661Leu
XM_006717121.3:c.1983C>G	XP_006717184.1:p.Phe661Leu
XM_017014762.1:c.2394C>G	XP_016870251.1:p.Phe798Leu
XM_017014763.1:c.1983C>G	XP_016870252.1:p.Phe661Leu
NM_004560.4:c.2403C>G MANE Select	NP_004551.2:p.Phe801Leu