Canonical Allele Identifier: CA410712283
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs1457325051
gnomAD v2: 22-20229969-C-G
gnomAD v4: 22-20242446-C-G
MyVariant Identifiers: chr22:g.20229969C>G (hg19) chr22:g.20242446C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242446C>G , CM000684.2:g.20242446C>G GRCh38
NC_000022.10:g.20229969C>G , CM000684.1:g.20229969C>G GRCh37
NC_000022.9:g.18609969C>G NCBI36
NG_012176.1:g.30848G>C
NG_012176.2:g.30848G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.687G>C MANE Select ENSP00000043402.7:p.Met229Ile
ENST00000043402.7:c.687G>C ENSP00000043402.7:p.Met229Ile
ENST00000416372.5:c.746G>C
ENST00000425986.1:c.944G>C
NM_023004.5:c.687G>C NP_075380.1:p.Met229Ile
NM_023004.6:c.687G>C MANE Select NP_075380.1:p.Met229Ile
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