Canonical Allele Identifier: CA5121061

Gene: ROR2

Linked Data

• dbSNP Id: rs201295111
• ExAC: 9:94519697 C / T
• gnomAD v2: 9-94519697-C-T
• gnomAD v3: 9-91757415-C-T
• gnomAD v4: 9-91757415-C-T
• COSMIC: COSM4722407
• MyVariant Identifiers: chr9:g.94519697C>T (hg19) ; chr9:g.91757415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757415C>T , CM000671.2:g.91757415C>T	GRCh38
NC_000009.11:g.94519697C>T , CM000671.1:g.94519697C>T	GRCh37
NC_000009.10:g.93559518C>T	NCBI36
NG_008089.1:g.197748G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.320G>A MANE Select	ENSP00000364860.3:p.Arg107Gln
ENST00000375708.3:c.320G>A	ENSP00000364860.3:p.Arg107Gln
ENST00000375715.5:c.-101G>A	ENSP00000364867.1:n.-101G>A
ENST00000495386.5:n.583G>A
ENST00000548585.2:n.172+14G>A
ENST00000550066.5:n.788G>A
NM_004560.3:c.320G>A	NP_004551.2:p.Arg107Gln
XM_005252008.3:c.-101G>A	XP_005252065.1:n.-101G>A
XM_006717121.2:c.-101G>A	XP_006717184.1:n.-101G>A
XM_011518721.1:c.-101G>A	XP_011517023.1:n.-101G>A
NM_001318204.1:c.320G>A	NP_001305133.1:p.Arg107Gln
XM_005252008.4:c.-101G>A	XP_005252065.1:n.-101G>A
XM_006717121.3:c.-101G>A	XP_006717184.1:n.-101G>A
XM_017014762.1:c.311G>A	XP_016870251.1:p.Arg104Gln
XM_017014763.1:c.-101G>A	XP_016870252.1:n.-101G>A
XR_001746315.1:n.563G>A
NM_004560.4:c.320G>A MANE Select	NP_004551.2:p.Arg107Gln
NM_001318204.2:c.320G>A	NP_001305133.1:p.Arg107Gln