Canonical Allele Identifier: CA410712494
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230072T>A (hg19) chr22:g.20242549T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242549T>A , CM000684.2:g.20242549T>A GRCh38
NC_000022.10:g.20230072T>A , CM000684.1:g.20230072T>A GRCh37
NC_000022.9:g.18610072T>A NCBI36
NG_012176.1:g.30745A>T
NG_012176.2:g.30745A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.584A>T MANE Select ENSP00000043402.7:p.Glu195Val
ENST00000043402.7:c.584A>T ENSP00000043402.7:p.Glu195Val
ENST00000416372.5:c.643A>T
ENST00000425986.1:c.841A>T
NM_023004.5:c.584A>T NP_075380.1:p.Glu195Val
NM_023004.6:c.584A>T MANE Select NP_075380.1:p.Glu195Val
Search 100 bp 5'
Search 100 bp 3'