Canonical Allele Identifier: CA513693647
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20229981A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242458A>G , CM000684.2:g.20242458A>G GRCh38
NC_000022.10:g.20229981A>G , CM000684.1:g.20229981A>G GRCh37
NC_000022.9:g.18609981A>G NCBI36
NG_012176.1:g.30836T>C
NG_012176.2:g.30836T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.675T>C MANE Select ENSP00000043402.7:p.Leu225=
ENST00000043402.7:c.675T>C ENSP00000043402.7:p.Leu225=
ENST00000416372.5:c.734T>C
ENST00000425986.1:c.932T>C
NM_023004.5:c.675T>C NP_075380.1:p.Leu225=
NM_023004.6:c.675T>C MANE Select NP_075380.1:p.Leu225=
Search 100 bp 5'
Search 100 bp 3'