Canonical Allele Identifier: CA2396269098
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242547G= , CM000684.2:g.20242547G= GRCh38
NC_000022.10:g.20230070G= , CM000684.1:g.20230070G= GRCh37
NC_000022.9:g.18610070G= NCBI36
NG_012176.1:g.30747C=
NG_012176.2:g.30747C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.586C= MANE Select ENSP00000043402.7:p.Arg196=
ENST00000043402.7:c.586C= ENSP00000043402.7:p.Arg196=
ENST00000416372.5:c.645C=
ENST00000425986.1:c.843C=
NM_023004.5:c.586C= NP_075380.1:p.Arg196=
NM_023004.6:c.586C= MANE Select NP_075380.1:p.Arg196=