Linked Data
dbSNP Id:
rs551516761
gnomAD v2:
1-206944505-T-C
gnomAD v3:
1-206771160-T-C
gnomAD v4:
1-206771160-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206771160T>C , CM000663.2:g.206771160T>C | GRCh38 |
| NC_000001.10:g.206944505T>C , CM000663.1:g.206944505T>C | GRCh37 |
| NC_000001.9:g.205011128T>C | NCBI36 |
| NG_012088.1:g.6335A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367099.4:n.30A>G (IL10) | ||
| ENST00000471071.2:c.-131A>G (IL10) | ENSP00000493073.2:n.-131A>G | |
| ENST00000659065.2:c.109-101A>G (IL10) | ENSP00000499588.1:n.109-101A>G | |
| ENST00000659642.2:c.109-101A>G (IL10) | ENSP00000499509.1:n.109-101A>G | |
| ENST00000664374.2:c.109-101A>G (IL10) | ENSP00000499664.1:n.109-101A>G | |
| ENST00000659997.3:c.-149+82T>C (IL19) MANE Select | ENSP00000499459.2:n.-149+82T>C | |
| ENST00000656872.2:c.-149+330T>C (IL19) | ENSP00000499487.2:n.-149+330T>C | |
| ENST00000659065.1:c.109-101A>G (IL10) | ENSP00000499588.1:n.109-101A>G | |
| ENST00000659642.1:c.109-101A>G (IL10) | ENSP00000499509.1:n.109-101A>G | |
| ENST00000659997.2:c.-149+82T>C (IL19) | ENSP00000499459.2:n.-149+82T>C | |
| ENST00000662320.1:n.67+330T>C (IL19) | ||
| ENST00000664374.1:c.109-101A>G (IL10) | ENSP00000499664.1:n.109-101A>G | |
| ENST00000367099.3:n.30A>G (IL10) | ||
| ENST00000423557.1:c.226-101A>G (IL10) MANE Select | ENSP00000412237.1:n.226-101A>G | |
| ENST00000471071.1:n.40A>G (IL10) | ||
| NM_000572.2:c.226-101A>G (IL10) | NP_000563.1:n.226-101A>G | |
| XM_011509506.1:c.226-101A>G (IL10) | XP_011507808.1:n.226-101A>G | |
| NM_000572.3:c.226-101A>G (IL10) MANE Select | NP_000563.1:n.226-101A>G | |
| NM_153758.3:c.-35+82T>C (IL19) | NP_715639.1:n.-35+82T>C | |
| NM_001382624.1:c.-131A>G (IL10) | NP_001369553.1:n.-131A>G | |
| NM_001393490.1:c.-149+330T>C (IL19) | NP_001380419.1:n.-149+330T>C | |
| NM_153758.5:c.-149+82T>C (IL19) MANE Select | NP_715639.2:n.-149+82T>C | |
| NR_168466.1:n.285-101A>G (IL10) |