Canonical Allele Identifier: CA410712278
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20229967G>T (hg19) chr22:g.20242444G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242444G>T , CM000684.2:g.20242444G>T GRCh38
NC_000022.10:g.20229967G>T , CM000684.1:g.20229967G>T GRCh37
NC_000022.9:g.18609967G>T NCBI36
NG_012176.1:g.30850C>A
NG_012176.2:g.30850C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.689C>A MANE Select ENSP00000043402.7:p.Thr230Lys
ENST00000043402.7:c.689C>A ENSP00000043402.7:p.Thr230Lys
ENST00000416372.5:c.748C>A
ENST00000425986.1:c.946C>A
NM_023004.5:c.689C>A NP_075380.1:p.Thr230Lys
NM_023004.6:c.689C>A MANE Select NP_075380.1:p.Thr230Lys
Search 100 bp 5'
Search 100 bp 3'