Canonical Allele Identifier: CA410712819

Gene: RTN4R

Linked Data

• dbSNP Id: rs1602636722
• MyVariant Identifiers: chr22:g.20230177T>A (hg19) ; chr22:g.20242654T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242654T>A , CM000684.2:g.20242654T>A	GRCh38
NC_000022.10:g.20230177T>A , CM000684.1:g.20230177T>A	GRCh37
NC_000022.9:g.18610177T>A	NCBI36
NG_012176.1:g.30640A>T
NG_012176.2:g.30640A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.479A>T MANE Select	ENSP00000043402.7:p.Tyr160Phe
ENST00000043402.7:c.479A>T	ENSP00000043402.7:p.Tyr160Phe
ENST00000416372.5:c.538A>T
ENST00000425986.1:c.736A>T
ENST00000469601.1:n.615A>T
NM_023004.5:c.479A>T	NP_075380.1:p.Tyr160Phe
NM_023004.6:c.479A>T MANE Select	NP_075380.1:p.Tyr160Phe