Canonical Allele Identifier: CA410712328
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20229991A>T (hg19) chr22:g.20242468A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242468A>T , CM000684.2:g.20242468A>T GRCh38
NC_000022.10:g.20229991A>T , CM000684.1:g.20229991A>T GRCh37
NC_000022.9:g.18609991A>T NCBI36
NG_012176.1:g.30826T>A
NG_012176.2:g.30826T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.665T>A MANE Select ENSP00000043402.7:p.Phe222Tyr
ENST00000043402.7:c.665T>A ENSP00000043402.7:p.Phe222Tyr
ENST00000416372.5:c.724T>A
ENST00000425986.1:c.922T>A
NM_023004.5:c.665T>A NP_075380.1:p.Phe222Tyr
NM_023004.6:c.665T>A MANE Select NP_075380.1:p.Phe222Tyr
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