Canonical Allele Identifier: CA513693356
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230131G>C (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.525C>G MANE Select ENSP00000043402.7:p.Arg175=
ENST00000043402.7:c.525C>G ENSP00000043402.7:p.Arg175=
ENST00000416372.5:c.584C>G
ENST00000425986.1:c.782C>G
ENST00000469601.1:n.661C>G
NM_023004.5:c.525C>G NP_075380.1:p.Arg175=
NM_023004.6:c.525C>G MANE Select NP_075380.1:p.Arg175=
Search 100 bp 5'
Search 100 bp 3'