Canonical Allele Identifier: CA10109572
Gene: RTN4R HGNC NCBI

Linked Data

ClinVar Variation Id: 3030721
ClinVar RCV Id: RCV003893877
dbSNP Id: rs117955118

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242617G>C , CM000684.2:g.20242617G>C GRCh38
NC_000022.10:g.20230140G>C , CM000684.1:g.20230140G>C GRCh37
NC_000022.9:g.18610140G>C NCBI36
NG_012176.1:g.30677C>G
NG_012176.2:g.30677C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.516C>G MANE Select ENSP00000043402.7:p.Asp172Glu
ENST00000043402.7:c.516C>G ENSP00000043402.7:p.Asp172Glu
ENST00000416372.5:c.575C>G
ENST00000425986.1:c.773C>G
ENST00000469601.1:n.652C>G
NM_023004.5:c.516C>G NP_075380.1:p.Asp172Glu
NM_023004.6:c.516C>G MANE Select NP_075380.1:p.Asp172Glu