Canonical Allele Identifier: CA466334554

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486229C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723947C>T , CM000671.2:g.91723947C>T	GRCh38
NC_000009.11:g.94486229C>T , CM000671.1:g.94486229C>T	GRCh37
NC_000009.10:g.93526050C>T	NCBI36
NG_008089.1:g.231216G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2547G>A MANE Select	ENSP00000364860.3:p.Gln849=
ENST00000375708.3:c.2547G>A	ENSP00000364860.3:p.Gln849=
ENST00000375715.5:c.1920+207G>A	ENSP00000364867.1:n.1920+207G>A
ENST00000550066.5:n.3015G>A
NM_004560.3:c.2547G>A	NP_004551.2:p.Gln849=
XM_005252008.3:c.2127G>A	XP_005252065.1:p.Gln709=
XM_005252009.3:c.1344G>A	XP_005252066.1:p.Gln448=
XM_006717121.2:c.2127G>A	XP_006717184.1:p.Gln709=
XM_011518721.1:c.2127G>A	XP_011517023.1:p.Gln709=
XM_005252008.4:c.2127G>A	XP_005252065.1:p.Gln709=
XM_006717121.3:c.2127G>A	XP_006717184.1:p.Gln709=
XM_017014762.1:c.2538G>A	XP_016870251.1:p.Gln846=
XM_017014763.1:c.2127G>A	XP_016870252.1:p.Gln709=
NM_004560.4:c.2547G>A MANE Select	NP_004551.2:p.Gln849=