Canonical Allele Identifier: CA513693421
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230152T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242629T>C , CM000684.2:g.20242629T>C GRCh38
NC_000022.10:g.20230152T>C , CM000684.1:g.20230152T>C GRCh37
NC_000022.9:g.18610152T>C NCBI36
NG_012176.1:g.30665A>G
NG_012176.2:g.30665A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.504A>G MANE Select ENSP00000043402.7:p.Ala168=
ENST00000043402.7:c.504A>G ENSP00000043402.7:p.Ala168=
ENST00000416372.5:c.563A>G
ENST00000425986.1:c.761A>G
ENST00000469601.1:n.640A>G
NM_023004.5:c.504A>G NP_075380.1:p.Ala168=
NM_023004.6:c.504A>G MANE Select NP_075380.1:p.Ala168=
Search 100 bp 5'
Search 100 bp 3'