Canonical Allele Identifier: CA410713234
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230310C>G (hg19) chr22:g.20242787C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242787C>G , CM000684.2:g.20242787C>G GRCh38
NC_000022.10:g.20230310C>G , CM000684.1:g.20230310C>G GRCh37
NC_000022.9:g.18610310C>G NCBI36
NG_012176.1:g.30507G>C
NG_012176.2:g.30507G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.346G>C MANE Select ENSP00000043402.7:p.Ala116Pro
ENST00000043402.7:c.346G>C ENSP00000043402.7:p.Ala116Pro
ENST00000416372.5:c.405G>C
ENST00000425986.1:c.603G>C
ENST00000469601.1:n.482G>C
NM_023004.5:c.346G>C NP_075380.1:p.Ala116Pro
NM_023004.6:c.346G>C MANE Select NP_075380.1:p.Ala116Pro
Search 100 bp 5'
Search 100 bp 3'