Canonical Allele Identifier: CA466359554

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519780T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757498T>A , CM000671.2:g.91757498T>A	GRCh38
NC_000009.11:g.94519780T>A , CM000671.1:g.94519780T>A	GRCh37
NC_000009.10:g.93559601T>A	NCBI36
NG_008089.1:g.197665A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.237A>T MANE Select	ENSP00000364860.3:p.Ala79=
ENST00000375708.3:c.237A>T	ENSP00000364860.3:p.Ala79=
ENST00000375715.5:c.-184A>T	ENSP00000364867.1:n.-184A>T
ENST00000495386.5:n.500A>T
ENST00000546883.1:n.439A>T
ENST00000548585.2:n.103A>T
ENST00000550066.5:n.705A>T
NM_004560.3:c.237A>T	NP_004551.2:p.Ala79=
XM_005252008.3:c.-184A>T	XP_005252065.1:n.-184A>T
XM_006717121.2:c.-184A>T	XP_006717184.1:n.-184A>T
XM_011518721.1:c.-184A>T	XP_011517023.1:n.-184A>T
NM_001318204.1:c.237A>T	NP_001305133.1:p.Ala79=
XM_005252008.4:c.-184A>T	XP_005252065.1:n.-184A>T
XM_006717121.3:c.-184A>T	XP_006717184.1:n.-184A>T
XM_017014762.1:c.228A>T	XP_016870251.1:p.Ala76=
XM_017014763.1:c.-184A>T	XP_016870252.1:n.-184A>T
XR_001746315.1:n.480A>T
NM_004560.4:c.237A>T MANE Select	NP_004551.2:p.Ala79=
NM_001318204.2:c.237A>T	NP_001305133.1:p.Ala79=