Canonical Allele Identifier: CA466359284

Gene: ROR2

Linked Data

• gnomAD v4: 9-91757354-C-G
• MyVariant Identifiers: chr9:g.94519636C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757354C>G , CM000671.2:g.91757354C>G	GRCh38
NC_000009.11:g.94519636C>G , CM000671.1:g.94519636C>G	GRCh37
NC_000009.10:g.93559457C>G	NCBI36
NG_008089.1:g.197809G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.381G>C MANE Select	ENSP00000364860.3:p.Thr127=
ENST00000375708.3:c.381G>C	ENSP00000364860.3:p.Thr127=
ENST00000375715.5:c.-40G>C	ENSP00000364867.1:n.-40G>C
ENST00000495386.5:n.644G>C
ENST00000548585.2:n.172+75G>C
ENST00000550066.5:n.849G>C
NM_004560.3:c.381G>C	NP_004551.2:p.Thr127=
XM_005252008.3:c.-40G>C	XP_005252065.1:n.-40G>C
XM_006717121.2:c.-40G>C	XP_006717184.1:n.-40G>C
XM_011518721.1:c.-40G>C	XP_011517023.1:n.-40G>C
NM_001318204.1:c.381G>C	NP_001305133.1:p.Thr127=
XM_005252008.4:c.-40G>C	XP_005252065.1:n.-40G>C
XM_006717121.3:c.-40G>C	XP_006717184.1:n.-40G>C
XM_017014762.1:c.372G>C	XP_016870251.1:p.Thr124=
XM_017014763.1:c.-40G>C	XP_016870252.1:n.-40G>C
XR_001746315.1:n.624G>C
NM_004560.4:c.381G>C MANE Select	NP_004551.2:p.Thr127=
NM_001318204.2:c.381G>C	NP_001305133.1:p.Thr127=