Canonical Allele Identifier: CA410712446
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs2051114357
MyVariant Identifiers: chr22:g.20230048C>A (hg19) chr22:g.20242525C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242525C>A , CM000684.2:g.20242525C>A GRCh38
NC_000022.10:g.20230048C>A , CM000684.1:g.20230048C>A GRCh37
NC_000022.9:g.18610048C>A NCBI36
NG_012176.1:g.30769G>T
NG_012176.2:g.30769G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.608G>T MANE Select ENSP00000043402.7:p.Ser203Ile
ENST00000043402.7:c.608G>T ENSP00000043402.7:p.Ser203Ile
ENST00000416372.5:c.667G>T
ENST00000425986.1:c.865G>T
NM_023004.5:c.608G>T NP_075380.1:p.Ser203Ile
NM_023004.6:c.608G>T MANE Select NP_075380.1:p.Ser203Ile
Search 100 bp 5'
Search 100 bp 3'