Canonical Allele Identifier: CA513693452

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20229915G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242392G>T , CM000684.2:g.20242392G>T	GRCh38
NC_000022.10:g.20229915G>T , CM000684.1:g.20229915G>T	GRCh37
NC_000022.9:g.18609915G>T	NCBI36
NG_012176.1:g.30902C>A
NG_012176.2:g.30902C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.741C>A MANE Select	ENSP00000043402.7:p.Ala247=
ENST00000043402.7:c.741C>A	ENSP00000043402.7:p.Ala247=
ENST00000416372.5:c.800C>A
ENST00000425986.1:c.998C>A
NM_023004.5:c.741C>A	NP_075380.1:p.Ala247=
NM_023004.6:c.741C>A MANE Select	NP_075380.1:p.Ala247=