Canonical Allele Identifier: CA513693129
Gene: RTN4R HGNC NCBI

Linked Data

gnomAD v4: 22-20242536-A-G
MyVariant Identifiers: chr22:g.20230059A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242536A>G , CM000684.2:g.20242536A>G GRCh38
NC_000022.10:g.20230059A>G , CM000684.1:g.20230059A>G GRCh37
NC_000022.9:g.18610059A>G NCBI36
NG_012176.1:g.30758T>C
NG_012176.2:g.30758T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.597T>C MANE Select ENSP00000043402.7:p.Arg199=
ENST00000043402.7:c.597T>C ENSP00000043402.7:p.Arg199=
ENST00000416372.5:c.656T>C
ENST00000425986.1:c.854T>C
NM_023004.5:c.597T>C NP_075380.1:p.Arg199=
NM_023004.6:c.597T>C MANE Select NP_075380.1:p.Arg199=
Search 100 bp 5'
Search 100 bp 3'