Canonical Allele Identifier: CA410712723

Gene: RTN4R

Linked Data

• dbSNP Id: rs2051115255
• MyVariant Identifiers: chr22:g.20230150A>G (hg19) ; chr22:g.20242627A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242627A>G , CM000684.2:g.20242627A>G	GRCh38
NC_000022.10:g.20230150A>G , CM000684.1:g.20230150A>G	GRCh37
NC_000022.9:g.18610150A>G	NCBI36
NG_012176.1:g.30667T>C
NG_012176.2:g.30667T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.506T>C MANE Select	ENSP00000043402.7:p.Leu169Pro
ENST00000043402.7:c.506T>C	ENSP00000043402.7:p.Leu169Pro
ENST00000416372.5:c.565T>C
ENST00000425986.1:c.763T>C
ENST00000469601.1:n.642T>C
NM_023004.5:c.506T>C	NP_075380.1:p.Leu169Pro
NM_023004.6:c.506T>C MANE Select	NP_075380.1:p.Leu169Pro