Canonical Allele Identifier: CA10109609
Gene: RTN4R HGNC NCBI

Linked Data

ClinVar Variation Id: 3035729
ClinVar RCV Id: RCV003912144
dbSNP Id: rs149052299
ExAC: 22:20230317 G / A
gnomAD v2: 22-20230317-G-A
gnomAD v3: 22-20242794-G-A
gnomAD v4: 22-20242794-G-A
MyVariant Identifiers: chr22:g.20230317G>A (hg19) chr22:g.20242794G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242794G>A , CM000684.2:g.20242794G>A GRCh38
NC_000022.10:g.20230317G>A , CM000684.1:g.20230317G>A GRCh37
NC_000022.9:g.18610317G>A NCBI36
NG_012176.1:g.30500C>T
NG_012176.2:g.30500C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.339C>T MANE Select ENSP00000043402.7:p.Ser113=
ENST00000043402.7:c.339C>T ENSP00000043402.7:p.Ser113=
ENST00000416372.5:c.398C>T
ENST00000425986.1:c.596C>T
ENST00000469601.1:n.475C>T
NM_023004.5:c.339C>T NP_075380.1:p.Ser113=
NM_023004.6:c.339C>T MANE Select NP_075380.1:p.Ser113=
Search 100 bp 5'
Search 100 bp 3'