Canonical Allele Identifier: CA373840799

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519733C>G (hg19) ; chr9:g.91757451C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757451C>G , CM000671.2:g.91757451C>G	GRCh38
NC_000009.11:g.94519733C>G , CM000671.1:g.94519733C>G	GRCh37
NC_000009.10:g.93559554C>G	NCBI36
NG_008089.1:g.197712G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.284G>C MANE Select	ENSP00000364860.3:p.Trp95Ser
ENST00000375708.3:c.284G>C	ENSP00000364860.3:p.Trp95Ser
ENST00000375715.5:c.-137G>C	ENSP00000364867.1:n.-137G>C
ENST00000495386.5:n.547G>C
ENST00000546883.1:n.486G>C
ENST00000548585.2:n.150G>C
ENST00000550066.5:n.752G>C
NM_004560.3:c.284G>C	NP_004551.2:p.Trp95Ser
XM_005252008.3:c.-137G>C	XP_005252065.1:n.-137G>C
XM_006717121.2:c.-137G>C	XP_006717184.1:n.-137G>C
XM_011518721.1:c.-137G>C	XP_011517023.1:n.-137G>C
NM_001318204.1:c.284G>C	NP_001305133.1:p.Trp95Ser
XM_005252008.4:c.-137G>C	XP_005252065.1:n.-137G>C
XM_006717121.3:c.-137G>C	XP_006717184.1:n.-137G>C
XM_017014762.1:c.275G>C	XP_016870251.1:p.Trp92Ser
XM_017014763.1:c.-137G>C	XP_016870252.1:n.-137G>C
XR_001746315.1:n.527G>C
NM_004560.4:c.284G>C MANE Select	NP_004551.2:p.Trp95Ser
NM_001318204.2:c.284G>C	NP_001305133.1:p.Trp95Ser