Canonical Allele Identifier: CA466339110

Gene: ROR2

Linked Data

• dbSNP Id: rs2118617749
• gnomAD v4: 9-91724505-G-A
• MyVariant Identifiers: chr9:g.94486787G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724505G>A , CM000671.2:g.91724505G>A	GRCh38
NC_000009.11:g.94486787G>A , CM000671.1:g.94486787G>A	GRCh37
NC_000009.10:g.93526608G>A	NCBI36
NG_008089.1:g.230658C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1989C>T MANE Select	ENSP00000364860.3:p.Ala663=
ENST00000375708.3:c.1989C>T	ENSP00000364860.3:p.Ala663=
ENST00000375715.5:c.1569C>T	ENSP00000364867.1:p.Ala523=
ENST00000550066.5:n.2457C>T
NM_004560.3:c.1989C>T	NP_004551.2:p.Ala663=
XM_005252008.3:c.1569C>T	XP_005252065.1:p.Ala523=
XM_005252009.3:c.786C>T	XP_005252066.1:p.Ala262=
XM_006717121.2:c.1569C>T	XP_006717184.1:p.Ala523=
XM_011518721.1:c.1569C>T	XP_011517023.1:p.Ala523=
XM_005252008.4:c.1569C>T	XP_005252065.1:p.Ala523=
XM_006717121.3:c.1569C>T	XP_006717184.1:p.Ala523=
XM_017014762.1:c.1980C>T	XP_016870251.1:p.Ala660=
XM_017014763.1:c.1569C>T	XP_016870252.1:p.Ala523=
NM_004560.4:c.1989C>T MANE Select	NP_004551.2:p.Ala663=