Canonical Allele Identifier: CA410712404
Gene: RTN4R HGNC NCBI

Linked Data

gnomAD v4: 22-20242504-T-C
MyVariant Identifiers: chr22:g.20230027T>C (hg19) chr22:g.20242504T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242504T>C , CM000684.2:g.20242504T>C GRCh38
NC_000022.10:g.20230027T>C , CM000684.1:g.20230027T>C GRCh37
NC_000022.9:g.18610027T>C NCBI36
NG_012176.1:g.30790A>G
NG_012176.2:g.30790A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.629A>G MANE Select ENSP00000043402.7:p.His210Arg
ENST00000043402.7:c.629A>G ENSP00000043402.7:p.His210Arg
ENST00000416372.5:c.688A>G
ENST00000425986.1:c.886A>G
NM_023004.5:c.629A>G NP_075380.1:p.His210Arg
NM_023004.6:c.629A>G MANE Select NP_075380.1:p.His210Arg
Search 100 bp 5'
Search 100 bp 3'