Canonical Allele Identifier: CA2396269046
Gene: RTN4R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242413C= , CM000684.2:g.20242413C= GRCh38
NC_000022.10:g.20229936C= , CM000684.1:g.20229936C= GRCh37
NC_000022.9:g.18609936C= NCBI36
NG_012176.1:g.30881G=
NG_012176.2:g.30881G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.720G= MANE Select ENSP00000043402.7:p.Ala240=
ENST00000043402.7:c.720G= ENSP00000043402.7:p.Ala240=
ENST00000416372.5:c.779G=
ENST00000425986.1:c.977G=
NM_023004.5:c.720G= NP_075380.1:p.Ala240=
NM_023004.6:c.720G= MANE Select NP_075380.1:p.Ala240=
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Search 100 bp 3'