Canonical Allele Identifier: CA2396269047
Gene: RTN4R HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242414G= , CM000684.2:g.20242414G= GRCh38
NC_000022.10:g.20229937G= , CM000684.1:g.20229937G= GRCh37
NC_000022.9:g.18609937G= NCBI36
NG_012176.1:g.30880C=
NG_012176.2:g.30880C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.719C= MANE Select ENSP00000043402.7:p.Ala240=
ENST00000043402.7:c.719C= ENSP00000043402.7:p.Ala240=
ENST00000416372.5:c.778C=
ENST00000425986.1:c.976C=
NM_023004.5:c.719C= NP_075380.1:p.Ala240=
NM_023004.6:c.719C= MANE Select NP_075380.1:p.Ala240=
Search 100 bp 5'
Search 100 bp 3'