Canonical Allele Identifier: CA513693578
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20229957C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242434C>T , CM000684.2:g.20242434C>T GRCh38
NC_000022.10:g.20229957C>T , CM000684.1:g.20229957C>T GRCh37
NC_000022.9:g.18609957C>T NCBI36
NG_012176.1:g.30860G>A
NG_012176.2:g.30860G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.699G>A MANE Select ENSP00000043402.7:p.Leu233=
ENST00000043402.7:c.699G>A ENSP00000043402.7:p.Leu233=
ENST00000416372.5:c.758G>A
ENST00000425986.1:c.956G>A
NM_023004.5:c.699G>A NP_075380.1:p.Leu233=
NM_023004.6:c.699G>A MANE Select NP_075380.1:p.Leu233=
Search 100 bp 5'
Search 100 bp 3'