Canonical Allele Identifier: CA513693165
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230305C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242782C>T , CM000684.2:g.20242782C>T GRCh38
NC_000022.10:g.20230305C>T , CM000684.1:g.20230305C>T GRCh37
NC_000022.9:g.18610305C>T NCBI36
NG_012176.1:g.30512G>A
NG_012176.2:g.30512G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.351G>A MANE Select ENSP00000043402.7:p.Gln117=
ENST00000043402.7:c.351G>A ENSP00000043402.7:p.Gln117=
ENST00000416372.5:c.410G>A
ENST00000425986.1:c.608G>A
ENST00000469601.1:n.487G>A
NM_023004.5:c.351G>A NP_075380.1:p.Gln117=
NM_023004.6:c.351G>A MANE Select NP_075380.1:p.Gln117=
Search 100 bp 5'
Search 100 bp 3'