gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.64466658 (AFR)
Genomes Max Group AF
0.64467438 (AFR)
Exomes Max Group AF
0.63346867 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118001371G>A , CM000673.2:g.118001371G>A | GRCh38 |
| NC_000011.9:g.117872086G>A , CM000673.1:g.117872086G>A | GRCh37 |
| NC_000011.8:g.117377296G>A | NCBI36 |
| NG_016275.1:g.19981G>A , LRG_151:g.19981G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525467.2:n.5254G>A (IL10RA) | ||
| ENST00000696732.1:n.5316G>A (IL10RA) | ||
| ENST00000227752.8:c.*1730G>A (IL10RA) MANE Select | ENSP00000227752.4:n.*1730G>A | |
| ENST00000529924.6:n.5045G>A (IL10RA) | ||
| ENST00000227752.7:c.*1730G>A (IL10RA) | ENSP00000227752.3:n.*1730G>A | |
| ENST00000529924.5:n.5045G>A (IL10RA) | ||
| NM_001558.3:c.*1730G>A , LRG_151t1:c.*1730G>A (IL10RA) | NP_001549.2:n.*1730G>A | |
| NR_026691.1:n.3674G>A (IL10RA) | ||
| XM_024448283.1:c.*5039C>T (SMIM35) | XP_024304051.1:n.*5039C>T | |
| XM_024448493.1:c.*1730G>A (IL10RA) | XP_024304261.1:n.*1730G>A | |
| XR_002957112.1:n.5693C>T (SMIM35) | ||
| XR_002957113.1:n.5209C>T (SMIM35) | ||
| NM_001558.4:c.*1730G>A (IL10RA) MANE Select | NP_001549.2:n.*1730G>A | |
| NR_026691.2:n.3671G>A (IL10RA) |