Canonical Allele Identifier: CA513693449

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230161C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242638C>G , CM000684.2:g.20242638C>G	GRCh38
NC_000022.10:g.20230161C>G , CM000684.1:g.20230161C>G	GRCh37
NC_000022.9:g.18610161C>G	NCBI36
NG_012176.1:g.30656G>C
NG_012176.2:g.30656G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.495G>C MANE Select	ENSP00000043402.7:p.Ala165=
ENST00000043402.7:c.495G>C	ENSP00000043402.7:p.Ala165=
ENST00000416372.5:c.554G>C
ENST00000425986.1:c.752G>C
ENST00000469601.1:n.631G>C
NM_023004.5:c.495G>C	NP_075380.1:p.Ala165=
NM_023004.6:c.495G>C MANE Select	NP_075380.1:p.Ala165=