Canonical Allele Identifier: CA513693170
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230308T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242785T>G , CM000684.2:g.20242785T>G GRCh38
NC_000022.10:g.20230308T>G , CM000684.1:g.20230308T>G GRCh37
NC_000022.9:g.18610308T>G NCBI36
NG_012176.1:g.30509A>C
NG_012176.2:g.30509A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.348A>C MANE Select ENSP00000043402.7:p.Ala116=
ENST00000043402.7:c.348A>C ENSP00000043402.7:p.Ala116=
ENST00000416372.5:c.407A>C
ENST00000425986.1:c.605A>C
ENST00000469601.1:n.484A>C
NM_023004.5:c.348A>C NP_075380.1:p.Ala116=
NM_023004.6:c.348A>C MANE Select NP_075380.1:p.Ala116=
Search 100 bp 5'
Search 100 bp 3'