Canonical Allele Identifier: CA2396269093
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242538G= , CM000684.2:g.20242538G= GRCh38
NC_000022.10:g.20230061G= , CM000684.1:g.20230061G= GRCh37
NC_000022.9:g.18610061G= NCBI36
NG_012176.1:g.30756C=
NG_012176.2:g.30756C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.595C= MANE Select ENSP00000043402.7:p.Arg199=
ENST00000043402.7:c.595C= ENSP00000043402.7:p.Arg199=
ENST00000416372.5:c.654C=
ENST00000425986.1:c.852C=
NM_023004.5:c.595C= NP_075380.1:p.Arg199=
NM_023004.6:c.595C= MANE Select NP_075380.1:p.Arg199=