Canonical Allele Identifier: CA513693167
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs1569034012
MyVariant Identifiers: chr22:g.20230308T>A (hg19)

Genomic Alleles

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

Transcript Alleles

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