Canonical Allele Identifier: CA10109568
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs140080129
ExAC: 22:20230131 G / A
gnomAD v2: 22-20230131-G-A
gnomAD v3: 22-20242608-G-A
gnomAD v4: 22-20242608-G-A
COSMIC: COSM4102711
MyVariant Identifiers: chr22:g.20230131G>A (hg19) chr22:g.20242608G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242608G>A , CM000684.2:g.20242608G>A GRCh38
NC_000022.10:g.20230131G>A , CM000684.1:g.20230131G>A GRCh37
NC_000022.9:g.18610131G>A NCBI36
NG_012176.1:g.30686C>T
NG_012176.2:g.30686C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.525C>T MANE Select ENSP00000043402.7:p.Arg175=
ENST00000043402.7:c.525C>T ENSP00000043402.7:p.Arg175=
ENST00000416372.5:c.584C>T
ENST00000425986.1:c.782C>T
ENST00000469601.1:n.661C>T
NM_023004.5:c.525C>T NP_075380.1:p.Arg175=
NM_023004.6:c.525C>T MANE Select NP_075380.1:p.Arg175=
Search 100 bp 5'
Search 100 bp 3'