Canonical Allele Identifier: CA373794275

Gene: ROR2

Linked Data

• ClinVar Variation Id: 1897777
• ClinVar RCV Id: RCV002569852
• dbSNP Id: rs1172192855
• gnomAD v2: 9-94486330-G-T
• gnomAD v3: 9-91724048-G-T
• gnomAD v4: 9-91724048-G-T
• MyVariant Identifiers: chr9:g.94486330G>T (hg19) ; chr9:g.91724048G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724048G>T , CM000671.2:g.91724048G>T	GRCh38
NC_000009.11:g.94486330G>T , CM000671.1:g.94486330G>T	GRCh37
NC_000009.10:g.93526151G>T	NCBI36
NG_008089.1:g.231115C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2446C>A MANE Select	ENSP00000364860.3:p.Gln816Lys
ENST00000375708.3:c.2446C>A	ENSP00000364860.3:p.Gln816Lys
ENST00000375715.5:c.1920+106C>A	ENSP00000364867.1:n.1920+106C>A
ENST00000550066.5:n.2914C>A
NM_004560.3:c.2446C>A	NP_004551.2:p.Gln816Lys
XM_005252008.3:c.2026C>A	XP_005252065.1:p.Gln676Lys
XM_005252009.3:c.1243C>A	XP_005252066.1:p.Gln415Lys
XM_006717121.2:c.2026C>A	XP_006717184.1:p.Gln676Lys
XM_011518721.1:c.2026C>A	XP_011517023.1:p.Gln676Lys
XM_005252008.4:c.2026C>A	XP_005252065.1:p.Gln676Lys
XM_006717121.3:c.2026C>A	XP_006717184.1:p.Gln676Lys
XM_017014762.1:c.2437C>A	XP_016870251.1:p.Gln813Lys
XM_017014763.1:c.2026C>A	XP_016870252.1:p.Gln676Lys
NM_004560.4:c.2446C>A MANE Select	NP_004551.2:p.Gln816Lys