Canonical Allele Identifier: CA410712285
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20229970A>C (hg19) chr22:g.20242447A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242447A>C , CM000684.2:g.20242447A>C GRCh38
NC_000022.10:g.20229970A>C , CM000684.1:g.20229970A>C GRCh37
NC_000022.9:g.18609970A>C NCBI36
NG_012176.1:g.30847T>G
NG_012176.2:g.30847T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.686T>G MANE Select ENSP00000043402.7:p.Met229Arg
ENST00000043402.7:c.686T>G ENSP00000043402.7:p.Met229Arg
ENST00000416372.5:c.745T>G
ENST00000425986.1:c.943T>G
NM_023004.5:c.686T>G NP_075380.1:p.Met229Arg
NM_023004.6:c.686T>G MANE Select NP_075380.1:p.Met229Arg
Search 100 bp 5'
Search 100 bp 3'