Canonical Allele Identifier: CA2396269052
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242422A= , CM000684.2:g.20242422A= GRCh38
NC_000022.10:g.20229945A= , CM000684.1:g.20229945A= GRCh37
NC_000022.9:g.18609945A= NCBI36
NG_012176.1:g.30872T=
NG_012176.2:g.30872T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.711T= MANE Select ENSP00000043402.7:p.Asn237=
ENST00000043402.7:c.711T= ENSP00000043402.7:p.Asn237=
ENST00000416372.5:c.770T=
ENST00000425986.1:c.968T=
NM_023004.5:c.711T= NP_075380.1:p.Asn237=
NM_023004.6:c.711T= MANE Select NP_075380.1:p.Asn237=