Canonical Allele Identifier: CA513693166
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230071C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242548C>T , CM000684.2:g.20242548C>T GRCh38
NC_000022.10:g.20230071C>T , CM000684.1:g.20230071C>T GRCh37
NC_000022.9:g.18610071C>T NCBI36
NG_012176.1:g.30746G>A
NG_012176.2:g.30746G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.585G>A MANE Select ENSP00000043402.7:p.Glu195=
ENST00000043402.7:c.585G>A ENSP00000043402.7:p.Glu195=
ENST00000416372.5:c.644G>A
ENST00000425986.1:c.842G>A
NM_023004.5:c.585G>A NP_075380.1:p.Glu195=
NM_023004.6:c.585G>A MANE Select NP_075380.1:p.Glu195=
Search 100 bp 5'
Search 100 bp 3'