Canonical Allele Identifier: CA10109533
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs752867645
ExAC: 22:20229939 T / C
gnomAD v2: 22-20229939-T-C
gnomAD v4: 22-20242416-T-C
MyVariant Identifiers: chr22:g.20229939T>C (hg19) chr22:g.20242416T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242416T>C , CM000684.2:g.20242416T>C GRCh38
NC_000022.10:g.20229939T>C , CM000684.1:g.20229939T>C GRCh37
NC_000022.9:g.18609939T>C NCBI36
NG_012176.1:g.30878A>G
NG_012176.2:g.30878A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.717A>G MANE Select ENSP00000043402.7:p.Ser239=
ENST00000043402.7:c.717A>G ENSP00000043402.7:p.Ser239=
ENST00000416372.5:c.776A>G
ENST00000425986.1:c.974A>G
NM_023004.5:c.717A>G NP_075380.1:p.Ser239=
NM_023004.6:c.717A>G MANE Select NP_075380.1:p.Ser239=
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