Canonical Allele Identifier: CA2396269081
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242503G= , CM000684.2:g.20242503G= GRCh38
NC_000022.10:g.20230026G= , CM000684.1:g.20230026G= GRCh37
NC_000022.9:g.18610026G= NCBI36
NG_012176.1:g.30791C=
NG_012176.2:g.30791C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.630C= MANE Select ENSP00000043402.7:p.His210=
ENST00000043402.7:c.630C= ENSP00000043402.7:p.His210=
ENST00000416372.5:c.689C=
ENST00000425986.1:c.887C=
NM_023004.5:c.630C= NP_075380.1:p.His210=
NM_023004.6:c.630C= MANE Select NP_075380.1:p.His210=