Canonical Allele Identifier: CA12992718

Gene: ROR2

Linked Data

• dbSNP Id: rs7048756
• gnomAD v2: 9-94612391-T-C
• gnomAD v3: 9-91850109-T-C
• gnomAD v4: 9-91850109-T-C
• MyVariant Identifiers: chr9:g.94612391T>C (hg19) ; chr9:g.91850109T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91850109T>C , CM000671.2:g.91850109T>C	GRCh38
NC_000009.11:g.94612391T>C , CM000671.1:g.94612391T>C	GRCh37
NC_000009.10:g.93652212T>C	NCBI36
NG_008089.1:g.105054A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.98-74291A>G MANE Select	ENSP00000364860.3:n.98-74291A>G
ENST00000375708.3:c.98-74291A>G	ENSP00000364860.3:n.98-74291A>G
ENST00000375715.5:c.-323-74291A>G	ENSP00000364867.1:n.-323-74291A>G
ENST00000495386.5:n.360+33149A>G
ENST00000546883.1:n.299+73656A>G
ENST00000550066.5:n.565+33149A>G
NM_004560.3:c.98-74291A>G	NP_004551.2:n.98-74291A>G
XM_005252008.3:c.-323-74291A>G	XP_005252065.1:n.-323-74291A>G
XM_011518721.1:c.-324+33149A>G	XP_011517023.1:n.-324+33149A>G
NM_001318204.1:c.98-74291A>G	NP_001305133.1:n.98-74291A>G
XM_005252008.4:c.-323-74291A>G	XP_005252065.1:n.-323-74291A>G
XM_017014763.1:c.-323-74291A>G	XP_016870252.1:n.-323-74291A>G
XR_001746315.1:n.341-74291A>G
NM_004560.4:c.98-74291A>G MANE Select	NP_004551.2:n.98-74291A>G
NM_001318204.2:c.98-74291A>G	NP_001305133.1:n.98-74291A>G