Canonical Allele Identifier: CA2396269069
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242474T= , CM000684.2:g.20242474T= GRCh38
NC_000022.10:g.20229997T= , CM000684.1:g.20229997T= GRCh37
NC_000022.9:g.18609997T= NCBI36
NG_012176.1:g.30820A=
NG_012176.2:g.30820A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.659A= MANE Select ENSP00000043402.7:p.His220=
ENST00000043402.7:c.659A= ENSP00000043402.7:p.His220=
ENST00000416372.5:c.718A=
ENST00000425986.1:c.916A=
NM_023004.5:c.659A= NP_075380.1:p.His220=
NM_023004.6:c.659A= MANE Select NP_075380.1:p.His220=