Canonical Allele Identifier: CA5120392

Gene: ROR2

Linked Data

• ClinVar Variation Id: 730222
• ClinVar RCV Id: RCV000904998
• dbSNP Id: rs200396791
• ExAC: 9:94486325 G / A
• gnomAD v2: 9-94486325-G-A
• gnomAD v3: 9-91724043-G-A
• gnomAD v4: 9-91724043-G-A
• MyVariant Identifiers: chr9:g.94486325G>A (hg19) ; chr9:g.91724043G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724043G>A , CM000671.2:g.91724043G>A	GRCh38
NC_000009.11:g.94486325G>A , CM000671.1:g.94486325G>A	GRCh37
NC_000009.10:g.93526146G>A	NCBI36
NG_008089.1:g.231120C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2451C>T MANE Select	ENSP00000364860.3:p.Leu817=
ENST00000375708.3:c.2451C>T	ENSP00000364860.3:p.Leu817=
ENST00000375715.5:c.1920+111C>T	ENSP00000364867.1:n.1920+111C>T
ENST00000550066.5:n.2919C>T
NM_004560.3:c.2451C>T	NP_004551.2:p.Leu817=
XM_005252008.3:c.2031C>T	XP_005252065.1:p.Leu677=
XM_005252009.3:c.1248C>T	XP_005252066.1:p.Leu416=
XM_006717121.2:c.2031C>T	XP_006717184.1:p.Leu677=
XM_011518721.1:c.2031C>T	XP_011517023.1:p.Leu677=
XM_005252008.4:c.2031C>T	XP_005252065.1:p.Leu677=
XM_006717121.3:c.2031C>T	XP_006717184.1:p.Leu677=
XM_017014762.1:c.2442C>T	XP_016870251.1:p.Leu814=
XM_017014763.1:c.2031C>T	XP_016870252.1:p.Leu677=
NM_004560.4:c.2451C>T MANE Select	NP_004551.2:p.Leu817=