Canonical Allele Identifier: CA513693476
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs930145807
gnomAD v2: 22-20230173-C-T
gnomAD v3: 22-20242650-C-T
gnomAD v4: 22-20242650-C-T
MyVariant Identifiers: chr22:g.20230173C>T (hg19) chr22:g.20242650C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242650C>T , CM000684.2:g.20242650C>T GRCh38
NC_000022.10:g.20230173C>T , CM000684.1:g.20230173C>T GRCh37
NC_000022.9:g.18610173C>T NCBI36
NG_012176.1:g.30644G>A
NG_012176.2:g.30644G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.483G>A MANE Select ENSP00000043402.7:p.Leu161=
ENST00000043402.7:c.483G>A ENSP00000043402.7:p.Leu161=
ENST00000416372.5:c.542G>A
ENST00000425986.1:c.740G>A
ENST00000469601.1:n.619G>A
NM_023004.5:c.483G>A NP_075380.1:p.Leu161=
NM_023004.6:c.483G>A MANE Select NP_075380.1:p.Leu161=
Search 100 bp 5'
Search 100 bp 3'