Canonical Allele Identifier: CA513693395
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230146A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242623A>C , CM000684.2:g.20242623A>C GRCh38
NC_000022.10:g.20230146A>C , CM000684.1:g.20230146A>C GRCh37
NC_000022.9:g.18610146A>C NCBI36
NG_012176.1:g.30671T>G
NG_012176.2:g.30671T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.510T>G MANE Select ENSP00000043402.7:p.Pro170=
ENST00000043402.7:c.510T>G ENSP00000043402.7:p.Pro170=
ENST00000416372.5:c.569T>G
ENST00000425986.1:c.767T>G
ENST00000469601.1:n.646T>G
NM_023004.5:c.510T>G NP_075380.1:p.Pro170=
NM_023004.6:c.510T>G MANE Select NP_075380.1:p.Pro170=
Search 100 bp 5'
Search 100 bp 3'