Canonical Allele Identifier: CA513693462

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20229918C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242395C>A , CM000684.2:g.20242395C>A	GRCh38
NC_000022.10:g.20229918C>A , CM000684.1:g.20229918C>A	GRCh37
NC_000022.9:g.18609918C>A	NCBI36
NG_012176.1:g.30899G>T
NG_012176.2:g.30899G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.738G>T MANE Select	ENSP00000043402.7:p.Leu246=
ENST00000043402.7:c.738G>T	ENSP00000043402.7:p.Leu246=
ENST00000416372.5:c.797G>T
ENST00000425986.1:c.995G>T
NM_023004.5:c.738G>T	NP_075380.1:p.Leu246=
NM_023004.6:c.738G>T MANE Select	NP_075380.1:p.Leu246=