Canonical Allele Identifier: CA589452464

Gene: ROR2

Linked Data

• dbSNP Id: rs991133932
• gnomAD v2: 9-94712289-G-C
• gnomAD v3: 9-91950007-G-C
• gnomAD v4: 9-91950007-G-C
• MyVariant Identifiers: chr9:g.94712289G>C (hg19) ; chr9:g.91950007G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91950007G>C , CM000671.2:g.91950007G>C	GRCh38
NC_000009.11:g.94712289G>C , CM000671.1:g.94712289G>C	GRCh37
NC_000009.10:g.93752110G>C	NCBI36
NG_008089.1:g.5156C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.-44C>G MANE Select	ENSP00000364860.3:n.-44C>G
ENST00000375708.3:c.-44C>G	ENSP00000364860.3:n.-44C>G
NM_004560.3:c.-44C>G	NP_004551.2:n.-44C>G
NM_001318204.1:c.-44C>G	NP_001305133.1:n.-44C>G
XR_001746315.1:n.200C>G
NM_004560.4:c.-44C>G MANE Select	NP_004551.2:n.-44C>G
NM_001318204.2:c.-44C>G	NP_001305133.1:n.-44C>G