Canonical Allele Identifier: CA513693270

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230347G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242824G>T , CM000684.2:g.20242824G>T	GRCh38
NC_000022.10:g.20230347G>T , CM000684.1:g.20230347G>T	GRCh37
NC_000022.9:g.18610347G>T	NCBI36
NG_012176.1:g.30470C>A
NG_012176.2:g.30470C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.309C>A MANE Select	ENSP00000043402.7:p.Gly103=
ENST00000043402.7:c.309C>A	ENSP00000043402.7:p.Gly103=
ENST00000416372.5:c.368C>A
ENST00000425986.1:c.566C>A
ENST00000469601.1:n.445C>A
NM_023004.5:c.309C>A	NP_075380.1:p.Gly103=
NM_023004.6:c.309C>A MANE Select	NP_075380.1:p.Gly103=