Canonical Allele Identifier: CA410713228
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230309G>A (hg19) chr22:g.20242786G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242786G>A , CM000684.2:g.20242786G>A GRCh38
NC_000022.10:g.20230309G>A , CM000684.1:g.20230309G>A GRCh37
NC_000022.9:g.18610309G>A NCBI36
NG_012176.1:g.30508C>T
NG_012176.2:g.30508C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.347C>T MANE Select ENSP00000043402.7:p.Ala116Val
ENST00000043402.7:c.347C>T ENSP00000043402.7:p.Ala116Val
ENST00000416372.5:c.406C>T
ENST00000425986.1:c.604C>T
ENST00000469601.1:n.483C>T
NM_023004.5:c.347C>T NP_075380.1:p.Ala116Val
NM_023004.6:c.347C>T MANE Select NP_075380.1:p.Ala116Val
Search 100 bp 5'
Search 100 bp 3'