Canonical Allele Identifier: CA410713536
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230400G>C (hg19) chr22:g.20242877G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242877G>C , CM000684.2:g.20242877G>C GRCh38
NC_000022.10:g.20230400G>C , CM000684.1:g.20230400G>C GRCh37
NC_000022.9:g.18610400G>C NCBI36
NG_012176.1:g.30417C>G
NG_012176.2:g.30417C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.256C>G MANE Select ENSP00000043402.7:p.Leu86Val
ENST00000043402.7:c.256C>G ENSP00000043402.7:p.Leu86Val
ENST00000416372.5:c.315C>G
ENST00000425986.1:c.513C>G
ENST00000469601.1:n.392C>G
ENST00000474642.1:n.531C>G
NM_023004.5:c.256C>G NP_075380.1:p.Leu86Val
NM_023004.6:c.256C>G MANE Select NP_075380.1:p.Leu86Val
Search 100 bp 5'
Search 100 bp 3'