Canonical Allele Identifier: CA10109535
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs764186010
ExAC: 22:20229957 C / G
gnomAD v2: 22-20229957-C-G
gnomAD v3: 22-20242434-C-G
gnomAD v4: 22-20242434-C-G
MyVariant Identifiers: chr22:g.20229957C>G (hg19) chr22:g.20242434C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242434C>G , CM000684.2:g.20242434C>G GRCh38
NC_000022.10:g.20229957C>G , CM000684.1:g.20229957C>G GRCh37
NC_000022.9:g.18609957C>G NCBI36
NG_012176.1:g.30860G>C
NG_012176.2:g.30860G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.699G>C MANE Select ENSP00000043402.7:p.Leu233=
ENST00000043402.7:c.699G>C ENSP00000043402.7:p.Leu233=
ENST00000416372.5:c.758G>C
ENST00000425986.1:c.956G>C
NM_023004.5:c.699G>C NP_075380.1:p.Leu233=
NM_023004.6:c.699G>C MANE Select NP_075380.1:p.Leu233=
Search 100 bp 5'
Search 100 bp 3'