Canonical Allele Identifier: CA465996322

Gene: ROR2

Linked Data

• gnomAD v4: 9-91726595-C-G
• MyVariant Identifiers: chr9:g.94488877C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726595C>G , CM000671.2:g.91726595C>G	GRCh38
NC_000009.11:g.94488877C>G , CM000671.1:g.94488877C>G	GRCh37
NC_000009.10:g.93528698C>G	NCBI36
NG_008089.1:g.228568G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1332G>C MANE Select	ENSP00000364860.3:p.Leu444=
ENST00000375708.3:c.1332G>C	ENSP00000364860.3:p.Leu444=
ENST00000375715.5:c.912G>C	ENSP00000364867.1:p.Leu304=
ENST00000550066.5:n.1800G>C
NM_004560.3:c.1332G>C	NP_004551.2:p.Leu444=
XM_005252008.3:c.912G>C	XP_005252065.1:p.Leu304=
XM_005252009.3:c.129G>C	XP_005252066.1:p.Leu43=
XM_006717121.2:c.912G>C	XP_006717184.1:p.Leu304=
XM_011518721.1:c.912G>C	XP_011517023.1:p.Leu304=
NM_001318204.1:c.1298G>C	NP_001305133.1:p.Ter433Ser
XM_005252008.4:c.912G>C	XP_005252065.1:p.Leu304=
XM_006717121.3:c.912G>C	XP_006717184.1:p.Leu304=
XM_017014762.1:c.1323G>C	XP_016870251.1:p.Leu441=
XM_017014763.1:c.912G>C	XP_016870252.1:p.Leu304=
XR_001746315.1:n.1541G>C
NM_004560.4:c.1332G>C MANE Select	NP_004551.2:p.Leu444=
NM_001318204.2:c.1298G>C	NP_001305133.1:p.Ter433Ser