Canonical Allele Identifier: CA410713204
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242780A>C , CM000684.2:g.20242780A>C GRCh38
NC_000022.10:g.20230303A>C , CM000684.1:g.20230303A>C GRCh37
NC_000022.9:g.18610303A>C NCBI36
NG_012176.1:g.30514T>G
NG_012176.2:g.30514T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.353T>G MANE Select ENSP00000043402.7:p.Leu118Arg
ENST00000043402.7:c.353T>G ENSP00000043402.7:p.Leu118Arg
ENST00000416372.5:c.412T>G
ENST00000425986.1:c.610T>G
ENST00000469601.1:n.489T>G
NM_023004.5:c.353T>G NP_075380.1:p.Leu118Arg
NM_023004.6:c.353T>G MANE Select NP_075380.1:p.Leu118Arg