Canonical Allele Identifier: CA410712685
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs1602636679

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242616T>G , CM000684.2:g.20242616T>G GRCh38
NC_000022.10:g.20230139T>G , CM000684.1:g.20230139T>G GRCh37
NC_000022.9:g.18610139T>G NCBI36
NG_012176.1:g.30678A>C
NG_012176.2:g.30678A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.517A>C MANE Select ENSP00000043402.7:p.Thr173Pro
ENST00000043402.7:c.517A>C ENSP00000043402.7:p.Thr173Pro
ENST00000416372.5:c.576A>C
ENST00000425986.1:c.774A>C
ENST00000469601.1:n.653A>C
NM_023004.5:c.517A>C NP_075380.1:p.Thr173Pro
NM_023004.6:c.517A>C MANE Select NP_075380.1:p.Thr173Pro