Linked Data
dbSNP Id:
rs3021094
gnomAD v2:
1-206944952-T-G
gnomAD v3:
1-206771607-T-G
gnomAD v4:
1-206771607-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206771607T>G , CM000663.2:g.206771607T>G | GRCh38 |
| NC_000001.10:g.206944952T>G , CM000663.1:g.206944952T>G | GRCh37 |
| NC_000001.9:g.205011575T>G | NCBI36 |
| NG_012088.1:g.5888A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000659065.2:c.49-192A>C (IL10) | ENSP00000499588.1:n.49-192A>C | |
| ENST00000659642.2:c.49-192A>C (IL10) | ENSP00000499509.1:n.49-192A>C | |
| ENST00000664374.2:c.49-192A>C (IL10) | ENSP00000499664.1:n.49-192A>C | |
| ENST00000659997.3:c.-149+529T>G (IL19) MANE Select | ENSP00000499459.2:n.-149+529T>G | |
| ENST00000656872.2:c.-149+777T>G (IL19) | ENSP00000499487.2:n.-149+777T>G | |
| ENST00000659065.1:c.49-192A>C (IL10) | ENSP00000499588.1:n.49-192A>C | |
| ENST00000659642.1:c.49-192A>C (IL10) | ENSP00000499509.1:n.49-192A>C | |
| ENST00000659997.2:c.-149+529T>G (IL19) | ENSP00000499459.2:n.-149+529T>G | |
| ENST00000662320.1:n.67+777T>G (IL19) | ||
| ENST00000664374.1:c.49-192A>C (IL10) | ENSP00000499664.1:n.49-192A>C | |
| ENST00000423557.1:c.166-192A>C (IL10) MANE Select | ENSP00000412237.1:n.166-192A>C | |
| NM_000572.2:c.166-192A>C (IL10) | NP_000563.1:n.166-192A>C | |
| XM_011509506.1:c.166-192A>C (IL10) | XP_011507808.1:n.166-192A>C | |
| NM_000572.3:c.166-192A>C (IL10) MANE Select | NP_000563.1:n.166-192A>C | |
| NM_153758.3:c.-35+529T>G (IL19) | NP_715639.1:n.-35+529T>G | |
| NM_001393490.1:c.-149+777T>G (IL19) | NP_001380419.1:n.-149+777T>G | |
| NM_153758.5:c.-149+529T>G (IL19) MANE Select | NP_715639.2:n.-149+529T>G | |
| NR_168466.1:n.225-192A>C (IL10) |