Canonical Allele Identifier: CA410712737
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242632C>A , CM000684.2:g.20242632C>A GRCh38
NC_000022.10:g.20230155C>A , CM000684.1:g.20230155C>A GRCh37
NC_000022.9:g.18610155C>A NCBI36
NG_012176.1:g.30662G>T
NG_012176.2:g.30662G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.501G>T MANE Select ENSP00000043402.7:p.Gln167His
ENST00000043402.7:c.501G>T ENSP00000043402.7:p.Gln167His
ENST00000416372.5:c.560G>T
ENST00000425986.1:c.758G>T
ENST00000469601.1:n.637G>T
NM_023004.5:c.501G>T NP_075380.1:p.Gln167His
NM_023004.6:c.501G>T MANE Select NP_075380.1:p.Gln167His