Canonical Allele Identifier: CA10109571
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs767594512
ExAC: 22:20230137 G / T
gnomAD v2: 22-20230137-G-T
gnomAD v4: 22-20242614-G-T
MyVariant Identifiers: chr22:g.20230137G>T (hg19) chr22:g.20242614G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242614G>T , CM000684.2:g.20242614G>T GRCh38
NC_000022.10:g.20230137G>T , CM000684.1:g.20230137G>T GRCh37
NC_000022.9:g.18610137G>T NCBI36
NG_012176.1:g.30680C>A
NG_012176.2:g.30680C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.519C>A MANE Select ENSP00000043402.7:p.Thr173=
ENST00000043402.7:c.519C>A ENSP00000043402.7:p.Thr173=
ENST00000416372.5:c.578C>A
ENST00000425986.1:c.776C>A
ENST00000469601.1:n.655C>A
NM_023004.5:c.519C>A NP_075380.1:p.Thr173=
NM_023004.6:c.519C>A MANE Select NP_075380.1:p.Thr173=
Search 100 bp 5'
Search 100 bp 3'