Canonical Allele Identifier: CA465996332

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488879G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726597G>A , CM000671.2:g.91726597G>A	GRCh38
NC_000009.11:g.94488879G>A , CM000671.1:g.94488879G>A	GRCh37
NC_000009.10:g.93528700G>A	NCBI36
NG_008089.1:g.228566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1330C>T MANE Select	ENSP00000364860.3:p.Leu444=
ENST00000375708.3:c.1330C>T	ENSP00000364860.3:p.Leu444=
ENST00000375715.5:c.910C>T	ENSP00000364867.1:p.Leu304=
ENST00000550066.5:n.1798C>T
NM_004560.3:c.1330C>T	NP_004551.2:p.Leu444=
XM_005252008.3:c.910C>T	XP_005252065.1:p.Leu304=
XM_005252009.3:c.127C>T	XP_005252066.1:p.Leu43=
XM_006717121.2:c.910C>T	XP_006717184.1:p.Leu304=
XM_011518721.1:c.910C>T	XP_011517023.1:p.Leu304=
NM_001318204.1:c.1296C>T	NP_001305133.1:p.Ser432=
XM_005252008.4:c.910C>T	XP_005252065.1:p.Leu304=
XM_006717121.3:c.910C>T	XP_006717184.1:p.Leu304=
XM_017014762.1:c.1321C>T	XP_016870251.1:p.Leu441=
XM_017014763.1:c.910C>T	XP_016870252.1:p.Leu304=
XR_001746315.1:n.1539C>T
NM_004560.4:c.1330C>T MANE Select	NP_004551.2:p.Leu444=
NM_001318204.2:c.1296C>T	NP_001305133.1:p.Ser432=