Canonical Allele Identifier: CA373796397

Gene: ROR2

Linked Data

• gnomAD v4: 9-91724452-A-C
• MyVariant Identifiers: chr9:g.94486734A>C (hg19) ; chr9:g.91724452A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724452A>C , CM000671.2:g.91724452A>C	GRCh38
NC_000009.11:g.94486734A>C , CM000671.1:g.94486734A>C	GRCh37
NC_000009.10:g.93526555A>C	NCBI36
NG_008089.1:g.230711T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2042T>G MANE Select	ENSP00000364860.3:p.Val681Gly
ENST00000375708.3:c.2042T>G	ENSP00000364860.3:p.Val681Gly
ENST00000375715.5:c.1622T>G	ENSP00000364867.1:p.Val541Gly
ENST00000550066.5:n.2510T>G
NM_004560.3:c.2042T>G	NP_004551.2:p.Val681Gly
XM_005252008.3:c.1622T>G	XP_005252065.1:p.Val541Gly
XM_005252009.3:c.839T>G	XP_005252066.1:p.Val280Gly
XM_006717121.2:c.1622T>G	XP_006717184.1:p.Val541Gly
XM_011518721.1:c.1622T>G	XP_011517023.1:p.Val541Gly
XM_005252008.4:c.1622T>G	XP_005252065.1:p.Val541Gly
XM_006717121.3:c.1622T>G	XP_006717184.1:p.Val541Gly
XM_017014762.1:c.2033T>G	XP_016870251.1:p.Val678Gly
XM_017014763.1:c.1622T>G	XP_016870252.1:p.Val541Gly
NM_004560.4:c.2042T>G MANE Select	NP_004551.2:p.Val681Gly