Canonical Allele Identifier: CA751515469
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs1296363363
gnomAD v3: 22-20242587-G-GC
gnomAD v4: 22-20242587-G-GC
MyVariant Identifiers: chr22:g.20230110_20230111insC (hg19) chr22:g.20242587_20242588insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242587_20242588insC , CM000684.2:g.20242587_20242588insC GRCh38
NC_000022.10:g.20230110_20230111insC , CM000684.1:g.20230110_20230111insC GRCh37
NC_000022.9:g.18610110_18610111insC NCBI36
NG_012176.1:g.30706_30707insG
NG_012176.2:g.30706_30707insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.545_546insG MANE Select ENSP00000043402.7:p.His182GlnfsTer?
ENST00000043402.7:c.545_546insG ENSP00000043402.7:p.His182GlnfsTer?
ENST00000416372.5:c.604_605insG
ENST00000425986.1:c.802_803insG
NM_023004.5:c.545_546insG NP_075380.1:p.His182GlnfsTer?
NM_023004.6:c.545_546insG MANE Select NP_075380.1:p.His182GlnfsTer?
Search 100 bp 5'
Search 100 bp 3'