Linked Data
dbSNP Id:
rs3024492
gnomAD v2:
1-206944112-T-A
gnomAD v3:
1-206770767-T-A
gnomAD v4:
1-206770767-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206770767T>A , CM000663.2:g.206770767T>A | GRCh38 |
| NC_000001.10:g.206944112T>A , CM000663.1:g.206944112T>A | GRCh37 |
| NC_000001.9:g.205010735T>A | NCBI36 |
| NG_012088.1:g.6728A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367099.4:n.283+140A>T (IL10) | ||
| ENST00000471071.2:c.123+140A>T (IL10) | ENSP00000493073.2:n.123+140A>T | |
| ENST00000659065.2:c.261+140A>T (IL10) | ENSP00000499588.1:n.261+140A>T | |
| ENST00000659642.2:c.261+140A>T (IL10) | ENSP00000499509.1:n.261+140A>T | |
| ENST00000664374.2:c.261+140A>T (IL10) | ENSP00000499664.1:n.261+140A>T | |
| ENST00000656872.2:c.-212T>A (IL19) | ENSP00000499487.2:n.-212T>A | |
| ENST00000659065.1:c.261+140A>T (IL10) | ENSP00000499588.1:n.261+140A>T | |
| ENST00000659642.1:c.261+140A>T (IL10) | ENSP00000499509.1:n.261+140A>T | |
| ENST00000659997.2:c.-460T>A (IL19) | ENSP00000499459.2:n.-460T>A | |
| ENST00000662320.1:n.4T>A (IL19) | ||
| ENST00000664374.1:c.261+140A>T (IL10) | ENSP00000499664.1:n.261+140A>T | |
| ENST00000367099.3:n.283+140A>T (IL10) | ||
| ENST00000423557.1:c.378+140A>T (IL10) MANE Select | ENSP00000412237.1:n.378+140A>T | |
| ENST00000471071.1:n.293+140A>T (IL10) | ||
| NM_000572.2:c.378+140A>T (IL10) | NP_000563.1:n.378+140A>T | |
| XM_011509506.1:c.378+140A>T (IL10) | XP_011507808.1:n.378+140A>T | |
| NM_000572.3:c.378+140A>T (IL10) MANE Select | NP_000563.1:n.378+140A>T | |
| NM_001382624.1:c.123+140A>T (IL10) | NP_001369553.1:n.123+140A>T | |
| NR_168466.1:n.437+140A>T (IL10) |