Canonical Allele Identifier: CA322183721
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs891231189

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242625G>T , CM000684.2:g.20242625G>T GRCh38
NC_000022.10:g.20230148G>T , CM000684.1:g.20230148G>T GRCh37
NC_000022.9:g.18610148G>T NCBI36
NG_012176.1:g.30669C>A
NG_012176.2:g.30669C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.508C>A MANE Select ENSP00000043402.7:p.Pro170Thr
ENST00000043402.7:c.508C>A ENSP00000043402.7:p.Pro170Thr
ENST00000416372.5:c.567C>A
ENST00000425986.1:c.765C>A
ENST00000469601.1:n.644C>A
NM_023004.5:c.508C>A NP_075380.1:p.Pro170Thr
NM_023004.6:c.508C>A MANE Select NP_075380.1:p.Pro170Thr