Canonical Allele Identifier: CA248106

Gene: ROR2

Linked Data

• ClinVar Variation Id: 159819
• ClinVar RCV Id: RCV000147390 ; RCV000180606 ; RCV000262682 ; RCV000513925
• dbSNP Id: rs41277835
• ExAC: 9:94485971 G / C
• gnomAD v2: 9-94485971-G-C
• gnomAD v3: 9-91723689-G-C
• gnomAD v4: 9-91723689-G-C
• MyVariant Identifiers: chr9:g.94485971G>C (hg19) ; chr9:g.91723689G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723689G>C , CM000671.2:g.91723689G>C	GRCh38
NC_000009.11:g.94485971G>C , CM000671.1:g.94485971G>C	GRCh37
NC_000009.10:g.93525792G>C	NCBI36
NG_008089.1:g.231474C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2805C>G MANE Select	ENSP00000364860.3:p.Asp935Glu
ENST00000375708.3:c.2805C>G	ENSP00000364860.3:p.Asp935Glu
ENST00000375715.5:c.1920+465C>G	ENSP00000364867.1:n.1920+465C>G
ENST00000550066.5:n.3273C>G
NM_004560.3:c.2805C>G	NP_004551.2:p.Asp935Glu
XM_005252008.3:c.2385C>G	XP_005252065.1:p.Asp795Glu
XM_005252009.3:c.1602C>G	XP_005252066.1:p.Asp534Glu
XM_006717121.2:c.2385C>G	XP_006717184.1:p.Asp795Glu
XM_011518721.1:c.2385C>G	XP_011517023.1:p.Asp795Glu
XM_005252008.4:c.2385C>G	XP_005252065.1:p.Asp795Glu
XM_006717121.3:c.2385C>G	XP_006717184.1:p.Asp795Glu
XM_017014762.1:c.2796C>G	XP_016870251.1:p.Asp932Glu
XM_017014763.1:c.2385C>G	XP_016870252.1:p.Asp795Glu
NM_004560.4:c.2805C>G MANE Select	NP_004551.2:p.Asp935Glu