Canonical Allele Identifier: CA410712756
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242637G>T , CM000684.2:g.20242637G>T GRCh38
NC_000022.10:g.20230160G>T , CM000684.1:g.20230160G>T GRCh37
NC_000022.9:g.18610160G>T NCBI36
NG_012176.1:g.30657C>A
NG_012176.2:g.30657C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.496C>A MANE Select ENSP00000043402.7:p.Leu166Met
ENST00000043402.7:c.496C>A ENSP00000043402.7:p.Leu166Met
ENST00000416372.5:c.555C>A
ENST00000425986.1:c.753C>A
ENST00000469601.1:n.632C>A
NM_023004.5:c.496C>A NP_075380.1:p.Leu166Met
NM_023004.6:c.496C>A MANE Select NP_075380.1:p.Leu166Met