Canonical Allele Identifier: CA513693482
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs1251935609
gnomAD v2: 22-20230176-G-A
gnomAD v4: 22-20242653-G-A
MyVariant Identifiers: chr22:g.20230176G>A (hg19) chr22:g.20242653G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242653G>A , CM000684.2:g.20242653G>A GRCh38
NC_000022.10:g.20230176G>A , CM000684.1:g.20230176G>A GRCh37
NC_000022.9:g.18610176G>A NCBI36
NG_012176.1:g.30641C>T
NG_012176.2:g.30641C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.480C>T MANE Select ENSP00000043402.7:p.Tyr160=
ENST00000043402.7:c.480C>T ENSP00000043402.7:p.Tyr160=
ENST00000416372.5:c.539C>T
ENST00000425986.1:c.737C>T
ENST00000469601.1:n.616C>T
NM_023004.5:c.480C>T NP_075380.1:p.Tyr160=
NM_023004.6:c.480C>T MANE Select NP_075380.1:p.Tyr160=
Search 100 bp 5'
Search 100 bp 3'