Canonical Allele Identifier: CA2396269035
Gene: RTN4R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242391G= , CM000684.2:g.20242391G= GRCh38
NC_000022.10:g.20229914G= , CM000684.1:g.20229914G= GRCh37
NC_000022.9:g.18609914G= NCBI36
NG_012176.1:g.30903C=
NG_012176.2:g.30903C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.742C= MANE Select ENSP00000043402.7:p.Pro248=
ENST00000043402.7:c.742C= ENSP00000043402.7:p.Pro248=
ENST00000416372.5:c.801C=
ENST00000425986.1:c.999C=
NM_023004.5:c.742C= NP_075380.1:p.Pro248=
NM_023004.6:c.742C= MANE Select NP_075380.1:p.Pro248=
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