Canonical Allele Identifier: CA410713235

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230310C>T (hg19) ; chr22:g.20242787C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242787C>T , CM000684.2:g.20242787C>T	GRCh38
NC_000022.10:g.20230310C>T , CM000684.1:g.20230310C>T	GRCh37
NC_000022.9:g.18610310C>T	NCBI36
NG_012176.1:g.30507G>A
NG_012176.2:g.30507G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000043402.8:c.346G>A MANE Select	ENSP00000043402.7:p.Ala116Thr
ENST00000043402.7:c.346G>A	ENSP00000043402.7:p.Ala116Thr
ENST00000416372.5:c.405G>A
ENST00000425986.1:c.603G>A
ENST00000469601.1:n.482G>A
NM_023004.5:c.346G>A	NP_075380.1:p.Ala116Thr
NM_023004.6:c.346G>A MANE Select	NP_075380.1:p.Ala116Thr