Canonical Allele Identifier: CA10109548
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs759879422
ExAC: 22:20230009 T / C
gnomAD v2: 22-20230009-T-C
gnomAD v3: 22-20242486-T-C
gnomAD v4: 22-20242486-T-C
MyVariant Identifiers: chr22:g.20230009T>C (hg19) chr22:g.20242486T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242486T>C , CM000684.2:g.20242486T>C GRCh38
NC_000022.10:g.20230009T>C , CM000684.1:g.20230009T>C GRCh37
NC_000022.9:g.18610009T>C NCBI36
NG_012176.1:g.30808A>G
NG_012176.2:g.30808A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.647A>G MANE Select ENSP00000043402.7:p.His216Arg
ENST00000043402.7:c.647A>G ENSP00000043402.7:p.His216Arg
ENST00000416372.5:c.706A>G
ENST00000425986.1:c.904A>G
NM_023004.5:c.647A>G NP_075380.1:p.His216Arg
NM_023004.6:c.647A>G MANE Select NP_075380.1:p.His216Arg
Search 100 bp 5'
Search 100 bp 3'