Canonical Allele Identifier: CA196010557

Gene: ROR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91950136C>G , CM000671.2:g.91950136C>G	GRCh38
NC_000009.11:g.94712418C>G , CM000671.1:g.94712418C>G	GRCh37
NC_000009.10:g.93752239C>G	NCBI36
NG_008089.1:g.5027G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.-173G>C MANE Select	ENSP00000364860.3:n.-173G>C
ENST00000375708.3:c.-173G>C	ENSP00000364860.3:n.-173G>C
NM_004560.3:c.-173G>C	NP_004551.2:n.-173G>C
NM_001318204.1:c.-173G>C	NP_001305133.1:n.-173G>C
XR_001746315.1:n.71G>C
NM_004560.4:c.-173G>C MANE Select	NP_004551.2:n.-173G>C
NM_001318204.2:c.-173G>C	NP_001305133.1:n.-173G>C