Canonical Allele Identifier: CA410712222
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242418A>G , CM000684.2:g.20242418A>G GRCh38
NC_000022.10:g.20229941A>G , CM000684.1:g.20229941A>G GRCh37
NC_000022.9:g.18609941A>G NCBI36
NG_012176.1:g.30876T>C
NG_012176.2:g.30876T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.715T>C MANE Select ENSP00000043402.7:p.Ser239Pro
ENST00000043402.7:c.715T>C ENSP00000043402.7:p.Ser239Pro
ENST00000416372.5:c.774T>C
ENST00000425986.1:c.972T>C
NM_023004.5:c.715T>C NP_075380.1:p.Ser239Pro
NM_023004.6:c.715T>C MANE Select NP_075380.1:p.Ser239Pro