Canonical Allele Identifier: CA410712251
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20229954A>C (hg19) chr22:g.20242431A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242431A>C , CM000684.2:g.20242431A>C GRCh38
NC_000022.10:g.20229954A>C , CM000684.1:g.20229954A>C GRCh37
NC_000022.9:g.18609954A>C NCBI36
NG_012176.1:g.30863T>G
NG_012176.2:g.30863T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.702T>G MANE Select ENSP00000043402.7:p.Phe234Leu
ENST00000043402.7:c.702T>G ENSP00000043402.7:p.Phe234Leu
ENST00000416372.5:c.761T>G
ENST00000425986.1:c.959T>G
NM_023004.5:c.702T>G NP_075380.1:p.Phe234Leu
NM_023004.6:c.702T>G MANE Select NP_075380.1:p.Phe234Leu
Search 100 bp 5'
Search 100 bp 3'