Canonical Allele Identifier: CA410713238
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230311A>C (hg19) chr22:g.20242788A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242788A>C , CM000684.2:g.20242788A>C GRCh38
NC_000022.10:g.20230311A>C , CM000684.1:g.20230311A>C GRCh37
NC_000022.9:g.18610311A>C NCBI36
NG_012176.1:g.30506T>G
NG_012176.2:g.30506T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.345T>G MANE Select ENSP00000043402.7:p.Asn115Lys
ENST00000043402.7:c.345T>G ENSP00000043402.7:p.Asn115Lys
ENST00000416372.5:c.404T>G
ENST00000425986.1:c.602T>G
ENST00000469601.1:n.481T>G
NM_023004.5:c.345T>G NP_075380.1:p.Asn115Lys
NM_023004.6:c.345T>G MANE Select NP_075380.1:p.Asn115Lys
Search 100 bp 5'
Search 100 bp 3'