Canonical Allele Identifier: CA513693440

Gene: RTN4R

Linked Data

• gnomAD v3: 22-20242635-C-T
• gnomAD v4: 22-20242635-C-T
• MyVariant Identifiers: chr22:g.20230158C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242635C>T , CM000684.2:g.20242635C>T	GRCh38
NC_000022.10:g.20230158C>T , CM000684.1:g.20230158C>T	GRCh37
NC_000022.9:g.18610158C>T	NCBI36
NG_012176.1:g.30659G>A
NG_012176.2:g.30659G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.498G>A MANE Select	ENSP00000043402.7:p.Leu166=
ENST00000043402.7:c.498G>A	ENSP00000043402.7:p.Leu166=
ENST00000416372.5:c.557G>A
ENST00000425986.1:c.755G>A
ENST00000469601.1:n.634G>A
NM_023004.5:c.498G>A	NP_075380.1:p.Leu166=
NM_023004.6:c.498G>A MANE Select	NP_075380.1:p.Leu166=