Canonical Allele Identifier: CA410713240
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230312T>A (hg19) chr22:g.20242789T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242789T>A , CM000684.2:g.20242789T>A GRCh38
NC_000022.10:g.20230312T>A , CM000684.1:g.20230312T>A GRCh37
NC_000022.9:g.18610312T>A NCBI36
NG_012176.1:g.30505A>T
NG_012176.2:g.30505A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.344A>T MANE Select ENSP00000043402.7:p.Asn115Ile
ENST00000043402.7:c.344A>T ENSP00000043402.7:p.Asn115Ile
ENST00000416372.5:c.403A>T
ENST00000425986.1:c.601A>T
ENST00000469601.1:n.480A>T
NM_023004.5:c.344A>T NP_075380.1:p.Asn115Ile
NM_023004.6:c.344A>T MANE Select NP_075380.1:p.Asn115Ile
Search 100 bp 5'
Search 100 bp 3'