Canonical Allele Identifier: CA10109564
Gene: RTN4R HGNC NCBI

Linked Data

ClinVar Variation Id: 3157060
ClinVar RCV Id: RCV004446903
dbSNP Id: rs746384572
ExAC: 22:20230091 G / A
gnomAD v2: 22-20230091-G-A
gnomAD v3: 22-20242568-G-A
gnomAD v4: 22-20242568-G-A
MyVariant Identifiers: chr22:g.20230091G>A (hg19) chr22:g.20242568G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242568G>A , CM000684.2:g.20242568G>A GRCh38
NC_000022.10:g.20230091G>A , CM000684.1:g.20230091G>A GRCh37
NC_000022.9:g.18610091G>A NCBI36
NG_012176.1:g.30726C>T
NG_012176.2:g.30726C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.565C>T MANE Select ENSP00000043402.7:p.Arg189Cys
ENST00000043402.7:c.565C>T ENSP00000043402.7:p.Arg189Cys
ENST00000416372.5:c.624C>T
ENST00000425986.1:c.822C>T
NM_023004.5:c.565C>T NP_075380.1:p.Arg189Cys
NM_023004.6:c.565C>T MANE Select NP_075380.1:p.Arg189Cys
Search 100 bp 5'
Search 100 bp 3'