Canonical Allele Identifier: CA410712340
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20229997T>A (hg19) chr22:g.20242474T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242474T>A , CM000684.2:g.20242474T>A GRCh38
NC_000022.10:g.20229997T>A , CM000684.1:g.20229997T>A GRCh37
NC_000022.9:g.18609997T>A NCBI36
NG_012176.1:g.30820A>T
NG_012176.2:g.30820A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.659A>T MANE Select ENSP00000043402.7:p.His220Leu
ENST00000043402.7:c.659A>T ENSP00000043402.7:p.His220Leu
ENST00000416372.5:c.718A>T
ENST00000425986.1:c.916A>T
NM_023004.5:c.659A>T NP_075380.1:p.His220Leu
NM_023004.6:c.659A>T MANE Select NP_075380.1:p.His220Leu
Search 100 bp 5'
Search 100 bp 3'