Canonical Allele Identifier: CA466334492

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486136G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723854G>A , CM000671.2:g.91723854G>A	GRCh38
NC_000009.11:g.94486136G>A , CM000671.1:g.94486136G>A	GRCh37
NC_000009.10:g.93525957G>A	NCBI36
NG_008089.1:g.231309C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2640C>T MANE Select	ENSP00000364860.3:p.Asn880=
ENST00000375708.3:c.2640C>T	ENSP00000364860.3:p.Asn880=
ENST00000375715.5:c.1920+300C>T	ENSP00000364867.1:n.1920+300C>T
ENST00000550066.5:n.3108C>T
NM_004560.3:c.2640C>T	NP_004551.2:p.Asn880=
XM_005252008.3:c.2220C>T	XP_005252065.1:p.Asn740=
XM_005252009.3:c.1437C>T	XP_005252066.1:p.Asn479=
XM_006717121.2:c.2220C>T	XP_006717184.1:p.Asn740=
XM_011518721.1:c.2220C>T	XP_011517023.1:p.Asn740=
XM_005252008.4:c.2220C>T	XP_005252065.1:p.Asn740=
XM_006717121.3:c.2220C>T	XP_006717184.1:p.Asn740=
XM_017014762.1:c.2631C>T	XP_016870251.1:p.Asn877=
XM_017014763.1:c.2220C>T	XP_016870252.1:p.Asn740=
NM_004560.4:c.2640C>T MANE Select	NP_004551.2:p.Asn880=