Canonical Allele Identifier: CA10109563
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs151151416

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242559T>C , CM000684.2:g.20242559T>C GRCh38
NC_000022.10:g.20230082T>C , CM000684.1:g.20230082T>C GRCh37
NC_000022.9:g.18610082T>C NCBI36
NG_012176.1:g.30735A>G
NG_012176.2:g.30735A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.574A>G MANE Select ENSP00000043402.7:p.Ser192Gly
ENST00000043402.7:c.574A>G ENSP00000043402.7:p.Ser192Gly
ENST00000416372.5:c.633A>G
ENST00000425986.1:c.831A>G
NM_023004.5:c.574A>G NP_075380.1:p.Ser192Gly
NM_023004.6:c.574A>G MANE Select NP_075380.1:p.Ser192Gly