Canonical Allele Identifier: CA322183677
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs866133447
gnomAD v2: 22-20230120-T-C
gnomAD v3: 22-20242597-T-C
gnomAD v4: 22-20242597-T-C
MyVariant Identifiers: chr22:g.20230120T>C (hg19) chr22:g.20242597T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242597T>C , CM000684.2:g.20242597T>C GRCh38
NC_000022.10:g.20230120T>C , CM000684.1:g.20230120T>C GRCh37
NC_000022.9:g.18610120T>C NCBI36
NG_012176.1:g.30697A>G
NG_012176.2:g.30697A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.536A>G MANE Select ENSP00000043402.7:p.Asn179Ser
ENST00000043402.7:c.536A>G ENSP00000043402.7:p.Asn179Ser
ENST00000416372.5:c.595A>G
ENST00000425986.1:c.793A>G
ENST00000469601.1:n.672A>G
NM_023004.5:c.536A>G NP_075380.1:p.Asn179Ser
NM_023004.6:c.536A>G MANE Select NP_075380.1:p.Asn179Ser
Search 100 bp 5'
Search 100 bp 3'