Canonical Allele Identifier: CA410712667
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242612A>C , CM000684.2:g.20242612A>C GRCh38
NC_000022.10:g.20230135A>C , CM000684.1:g.20230135A>C GRCh37
NC_000022.9:g.18610135A>C NCBI36
NG_012176.1:g.30682T>G
NG_012176.2:g.30682T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.521T>G MANE Select ENSP00000043402.7:p.Phe174Cys
ENST00000043402.7:c.521T>G ENSP00000043402.7:p.Phe174Cys
ENST00000416372.5:c.580T>G
ENST00000425986.1:c.778T>G
ENST00000469601.1:n.657T>G
NM_023004.5:c.521T>G NP_075380.1:p.Phe174Cys
NM_023004.6:c.521T>G MANE Select NP_075380.1:p.Phe174Cys