gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.95949732 (EAS)
Genomes Max Group AF
0.95949732 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.51083632T>C , CM000677.2:g.51083632T>C | GRCh38 |
| NC_000015.9:g.51375829T>C , CM000677.1:g.51375829T>C | GRCh37 |
| NC_000015.8:g.49163121T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000637513.2:c.52+10912A>G (TNFAIP8L3) MANE Select | ENSP00000489743.1:n.52+10912A>G | |
| ENST00000649177.1:c.-87+10779A>G (TNFAIP8L3) | ENSP00000498365.1:n.-87+10779A>G | |
| ENST00000327536.5:c.316+10912A>G (TNFAIP8L3) | ENSP00000328016.5:n.316+10912A>G | |
| NM_001311175.1:c.52+10912A>G (TNFAIP8L3) | NP_001298104.1:n.52+10912A>G | |
| NM_207381.3:c.316+10912A>G (TNFAIP8L3) | NP_997264.2:n.316+10912A>G | |
| XM_006720500.2:c.-87+1415A>G (TNFAIP8L3) | XP_006720563.1:n.-87+1415A>G | |
| XR_932222.1:n.98+45951T>C (PIRC66) | ||
| NR_146310.1:n.194+45951T>C (MIR4713HG) | ||
| XM_017022169.1:c.-87+1415A>G (TNFAIP8L3) | XP_016877658.1:n.-87+1415A>G | |
| NM_001311175.2:c.52+10912A>G (TNFAIP8L3) MANE Select | NP_001298104.1:n.52+10912A>G | |
| NM_207381.4:c.316+10912A>G (TNFAIP8L3) | NP_997264.2:n.316+10912A>G |