Linked Data
dbSNP Id:
rs753924360
ExAC:
1:206944418 C / A
gnomAD v2:
1-206944418-C-A
gnomAD v4:
1-206771073-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206771073C>A , CM000663.2:g.206771073C>A | GRCh38 |
| NC_000001.10:g.206944418C>A , CM000663.1:g.206944418C>A | GRCh37 |
| NC_000001.9:g.205011041C>A | NCBI36 |
| NG_012088.1:g.6422G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367099.4:n.117G>T (IL10) | ||
| ENST00000471071.2:c.-44G>T (IL10) | ENSP00000493073.2:n.-44G>T | |
| ENST00000659065.2:c.109-14G>T (IL10) | ENSP00000499588.1:n.109-14G>T | |
| ENST00000659642.2:c.109-14G>T (IL10) | ENSP00000499509.1:n.109-14G>T | |
| ENST00000664374.2:c.109-14G>T (IL10) | ENSP00000499664.1:n.109-14G>T | |
| ENST00000659997.3:c.-154C>A (IL19) MANE Select | ENSP00000499459.2:n.-154C>A | |
| ENST00000656872.2:c.-149+243C>A (IL19) | ENSP00000499487.2:n.-149+243C>A | |
| ENST00000659065.1:c.109-14G>T (IL10) | ENSP00000499588.1:n.109-14G>T | |
| ENST00000659642.1:c.109-14G>T (IL10) | ENSP00000499509.1:n.109-14G>T | |
| ENST00000659997.2:c.-154C>A (IL19) | ENSP00000499459.2:n.-154C>A | |
| ENST00000662320.1:n.67+243C>A (IL19) | ||
| ENST00000664374.1:c.109-14G>T (IL10) | ENSP00000499664.1:n.109-14G>T | |
| ENST00000367099.3:n.117G>T (IL10) | ||
| ENST00000423557.1:c.226-14G>T (IL10) MANE Select | ENSP00000412237.1:n.226-14G>T | |
| ENST00000471071.1:n.127G>T (IL10) | ||
| NM_000572.2:c.226-14G>T (IL10) | NP_000563.1:n.226-14G>T | |
| XM_011509506.1:c.226-14G>T (IL10) | XP_011507808.1:n.226-14G>T | |
| NM_000572.3:c.226-14G>T (IL10) MANE Select | NP_000563.1:n.226-14G>T | |
| NM_153758.3:c.-40C>A (IL19) | NP_715639.1:n.-40C>A | |
| NM_001382624.1:c.-44G>T (IL10) | NP_001369553.1:n.-44G>T | |
| NM_001393490.1:c.-149+243C>A (IL19) | NP_001380419.1:n.-149+243C>A | |
| NM_153758.5:c.-154C>A (IL19) MANE Select | NP_715639.2:n.-154C>A | |
| NR_168466.1:n.285-14G>T (IL10) |