Canonical Allele Identifier: CA513693047
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230034G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242511G>A , CM000684.2:g.20242511G>A GRCh38
NC_000022.10:g.20230034G>A , CM000684.1:g.20230034G>A GRCh37
NC_000022.9:g.18610034G>A NCBI36
NG_012176.1:g.30783C>T
NG_012176.2:g.30783C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.622C>T MANE Select ENSP00000043402.7:p.Leu208=
ENST00000043402.7:c.622C>T ENSP00000043402.7:p.Leu208=
ENST00000416372.5:c.681C>T
ENST00000425986.1:c.879C>T
NM_023004.5:c.622C>T NP_075380.1:p.Leu208=
NM_023004.6:c.622C>T MANE Select NP_075380.1:p.Leu208=
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