Canonical Allele Identifier: CA10109534
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs763031493
ExAC: 22:20229955 A / T
gnomAD v2: 22-20229955-A-T
MyVariant Identifiers: chr22:g.20229955A>T (hg19) chr22:g.20242432A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242432A>T , CM000684.2:g.20242432A>T GRCh38
NC_000022.10:g.20229955A>T , CM000684.1:g.20229955A>T GRCh37
NC_000022.9:g.18609955A>T NCBI36
NG_012176.1:g.30862T>A
NG_012176.2:g.30862T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.701T>A MANE Select ENSP00000043402.7:p.Phe234Tyr
ENST00000043402.7:c.701T>A ENSP00000043402.7:p.Phe234Tyr
ENST00000416372.5:c.760T>A
ENST00000425986.1:c.958T>A
NM_023004.5:c.701T>A NP_075380.1:p.Phe234Tyr
NM_023004.6:c.701T>A MANE Select NP_075380.1:p.Phe234Tyr
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