Canonical Allele Identifier: CA322184050
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs372599978
gnomAD v2: 22-20230311-A-G
gnomAD v3: 22-20242788-A-G
gnomAD v4: 22-20242788-A-G
MyVariant Identifiers: chr22:g.20230311A>G (hg19) chr22:g.20242788A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.345T>C MANE Select ENSP00000043402.7:p.Asn115=
ENST00000043402.7:c.345T>C ENSP00000043402.7:p.Asn115=
ENST00000416372.5:c.404T>C
ENST00000425986.1:c.602T>C
ENST00000469601.1:n.481T>C
NM_023004.5:c.345T>C NP_075380.1:p.Asn115=
NM_023004.6:c.345T>C MANE Select NP_075380.1:p.Asn115=
Search 100 bp 5'
Search 100 bp 3'