Canonical Allele Identifier: CA195321403

Gene: ROR2

Linked Data

• ClinVar Variation Id: 2957649
• ClinVar RCV Id: RCV003811312
• dbSNP Id: rs1057029126
• gnomAD v2: 9-94486029-T-G
• gnomAD v3: 9-91723747-T-G
• gnomAD v4: 9-91723747-T-G
• MyVariant Identifiers: chr9:g.94486029T>G (hg19) ; chr9:g.91723747T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723747T>G , CM000671.2:g.91723747T>G	GRCh38
NC_000009.11:g.94486029T>G , CM000671.1:g.94486029T>G	GRCh37
NC_000009.10:g.93525850T>G	NCBI36
NG_008089.1:g.231416A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2747A>C MANE Select	ENSP00000364860.3:p.Glu916Ala
ENST00000375708.3:c.2747A>C	ENSP00000364860.3:p.Glu916Ala
ENST00000375715.5:c.1920+407A>C	ENSP00000364867.1:n.1920+407A>C
ENST00000550066.5:n.3215A>C
NM_004560.3:c.2747A>C	NP_004551.2:p.Glu916Ala
XM_005252008.3:c.2327A>C	XP_005252065.1:p.Glu776Ala
XM_005252009.3:c.1544A>C	XP_005252066.1:p.Glu515Ala
XM_006717121.2:c.2327A>C	XP_006717184.1:p.Glu776Ala
XM_011518721.1:c.2327A>C	XP_011517023.1:p.Glu776Ala
XM_005252008.4:c.2327A>C	XP_005252065.1:p.Glu776Ala
XM_006717121.3:c.2327A>C	XP_006717184.1:p.Glu776Ala
XM_017014762.1:c.2738A>C	XP_016870251.1:p.Glu913Ala
XM_017014763.1:c.2327A>C	XP_016870252.1:p.Glu776Ala
NM_004560.4:c.2747A>C MANE Select	NP_004551.2:p.Glu916Ala