Linked Data
ClinVar Variation Id:
1166836
dbSNP Id:
rs1800871
gnomAD v2:
1-206946634-A-G
gnomAD v3:
1-206773289-A-G
gnomAD v4:
1-206773289-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206773289A>G , CM000663.2:g.206773289A>G | GRCh38 |
| NC_000001.10:g.206946634A>G , CM000663.1:g.206946634A>G | GRCh37 |
| NC_000001.9:g.205013257A>G | NCBI36 |
| NG_012088.1:g.4206T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000659065.2:c.-15+391T>C (IL10) | ENSP00000499588.1:n.-15+391T>C | |
| ENST00000659642.2:c.-971T>C (IL10) | ENSP00000499509.1:n.-971T>C | |
| ENST00000664374.2:c.-14-957T>C (IL10) | ENSP00000499664.1:n.-14-957T>C | |
| ENST00000659997.3:c.-149+2211A>G (IL19) MANE Select | ENSP00000499459.2:n.-149+2211A>G | |
| ENST00000656872.2:c.-149+2459A>G (IL19) | ENSP00000499487.2:n.-149+2459A>G | |
| ENST00000659065.1:c.-15+391T>C (IL10) | ENSP00000499588.1:n.-15+391T>C | |
| ENST00000659642.1:c.-971T>C (IL10) | ENSP00000499509.1:n.-971T>C | |
| ENST00000659997.2:c.-149+2211A>G (IL19) | ENSP00000499459.2:n.-149+2211A>G | |
| ENST00000662320.1:n.67+2459A>G (IL19) | ||
| ENST00000664374.1:c.-14-957T>C (IL10) | ENSP00000499664.1:n.-14-957T>C | |
| XM_011509506.1:c.-854T>C (IL10) | XP_011507808.1:n.-854T>C | |
| NM_153758.3:c.-35+2211A>G (IL19) | NP_715639.1:n.-35+2211A>G | |
| NM_001393490.1:c.-149+2459A>G (IL19) | NP_001380419.1:n.-149+2459A>G | |
| NM_153758.5:c.-149+2211A>G (IL19) MANE Select | NP_715639.2:n.-149+2211A>G |