Canonical Allele Identifier: CA373796794

Gene: ROR2

Linked Data

• ClinVar Variation Id: 595513
• ClinVar RCV Id: RCV000731077
• dbSNP Id: rs1239750233
• gnomAD v2: 9-94486810-T-C
• gnomAD v4: 9-91724528-T-C
• MyVariant Identifiers: chr9:g.94486810T>C (hg19) ; chr9:g.91724528T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724528T>C , CM000671.2:g.91724528T>C	GRCh38
NC_000009.11:g.94486810T>C , CM000671.1:g.94486810T>C	GRCh37
NC_000009.10:g.93526631T>C	NCBI36
NG_008089.1:g.230635A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1966A>G MANE Select	ENSP00000364860.3:p.Ile656Val
ENST00000375708.3:c.1966A>G	ENSP00000364860.3:p.Ile656Val
ENST00000375715.5:c.1546A>G	ENSP00000364867.1:p.Ile516Val
ENST00000550066.5:n.2434A>G
NM_004560.3:c.1966A>G	NP_004551.2:p.Ile656Val
XM_005252008.3:c.1546A>G	XP_005252065.1:p.Ile516Val
XM_005252009.3:c.763A>G	XP_005252066.1:p.Ile255Val
XM_006717121.2:c.1546A>G	XP_006717184.1:p.Ile516Val
XM_011518721.1:c.1546A>G	XP_011517023.1:p.Ile516Val
XM_005252008.4:c.1546A>G	XP_005252065.1:p.Ile516Val
XM_006717121.3:c.1546A>G	XP_006717184.1:p.Ile516Val
XM_017014762.1:c.1957A>G	XP_016870251.1:p.Ile653Val
XM_017014763.1:c.1546A>G	XP_016870252.1:p.Ile516Val
NM_004560.4:c.1966A>G MANE Select	NP_004551.2:p.Ile656Val