Canonical Allele Identifier: CA2396269085
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242516C= , CM000684.2:g.20242516C= GRCh38
NC_000022.10:g.20230039C= , CM000684.1:g.20230039C= GRCh37
NC_000022.9:g.18610039C= NCBI36
NG_012176.1:g.30778G=
NG_012176.2:g.30778G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.617G= MANE Select ENSP00000043402.7:p.Arg206=
ENST00000043402.7:c.617G= ENSP00000043402.7:p.Arg206=
ENST00000416372.5:c.676G=
ENST00000425986.1:c.874G=
NM_023004.5:c.617G= NP_075380.1:p.Arg206=
NM_023004.6:c.617G= MANE Select NP_075380.1:p.Arg206=