Canonical Allele Identifier: CA465995413

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94485989A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723707A>G , CM000671.2:g.91723707A>G	GRCh38
NC_000009.11:g.94485989A>G , CM000671.1:g.94485989A>G	GRCh37
NC_000009.10:g.93525810A>G	NCBI36
NG_008089.1:g.231456T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2787T>C MANE Select	ENSP00000364860.3:p.Cys929=
ENST00000375708.3:c.2787T>C	ENSP00000364860.3:p.Cys929=
ENST00000375715.5:c.1920+447T>C	ENSP00000364867.1:n.1920+447T>C
ENST00000550066.5:n.3255T>C
NM_004560.3:c.2787T>C	NP_004551.2:p.Cys929=
XM_005252008.3:c.2367T>C	XP_005252065.1:p.Cys789=
XM_005252009.3:c.1584T>C	XP_005252066.1:p.Cys528=
XM_006717121.2:c.2367T>C	XP_006717184.1:p.Cys789=
XM_011518721.1:c.2367T>C	XP_011517023.1:p.Cys789=
XM_005252008.4:c.2367T>C	XP_005252065.1:p.Cys789=
XM_006717121.3:c.2367T>C	XP_006717184.1:p.Cys789=
XM_017014762.1:c.2778T>C	XP_016870251.1:p.Cys926=
XM_017014763.1:c.2367T>C	XP_016870252.1:p.Cys789=
NM_004560.4:c.2787T>C MANE Select	NP_004551.2:p.Cys929=