Linked Data
dbSNP Id:
rs758058722
ExAC:
1:206944328 T / C
gnomAD v2:
1-206944328-T-C
gnomAD v3:
1-206770983-T-C
gnomAD v4:
1-206770983-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206770983T>C , CM000663.2:g.206770983T>C | GRCh38 |
| NC_000001.10:g.206944328T>C , CM000663.1:g.206944328T>C | GRCh37 |
| NC_000001.9:g.205010951T>C | NCBI36 |
| NG_012088.1:g.6512A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367099.4:n.207A>G (IL10) | ||
| ENST00000471071.2:c.47A>G (IL10) | ENSP00000493073.2:p.Gln16Arg | |
| ENST00000659065.2:c.185A>G (IL10) | ENSP00000499588.1:p.Gln62Arg | |
| ENST00000659642.2:c.185A>G (IL10) | ENSP00000499509.1:p.Gln62Arg | |
| ENST00000664374.2:c.185A>G (IL10) | ENSP00000499664.1:p.Gln62Arg | |
| ENST00000659997.3:c.-244T>C (IL19) MANE Select | ENSP00000499459.2:n.-244T>C | |
| ENST00000656872.2:c.-149+153T>C (IL19) | ENSP00000499487.2:n.-149+153T>C | |
| ENST00000659065.1:c.185A>G (IL10) | ENSP00000499588.1:p.Gln62Arg | |
| ENST00000659642.1:c.185A>G (IL10) | ENSP00000499509.1:p.Gln62Arg | |
| ENST00000659997.2:c.-244T>C (IL19) | ENSP00000499459.2:n.-244T>C | |
| ENST00000662320.1:n.67+153T>C (IL19) | ||
| ENST00000664374.1:c.185A>G (IL10) | ENSP00000499664.1:p.Gln62Arg | |
| ENST00000367099.3:n.207A>G (IL10) | ||
| ENST00000423557.1:c.302A>G (IL10) MANE Select | ENSP00000412237.1:p.Gln101Arg | |
| ENST00000471071.1:n.217A>G (IL10) | ||
| NM_000572.2:c.302A>G (IL10) | NP_000563.1:p.Gln101Arg | |
| XM_011509506.1:c.302A>G (IL10) | XP_011507808.1:p.Gln101Arg | |
| NM_000572.3:c.302A>G (IL10) MANE Select | NP_000563.1:p.Gln101Arg | |
| NM_153758.3:c.-130T>C (IL19) | NP_715639.1:n.-130T>C | |
| NM_001382624.1:c.47A>G (IL10) | NP_001369553.1:p.Gln16Arg | |
| NM_001393490.1:c.-149+153T>C (IL19) | NP_001380419.1:n.-149+153T>C | |
| NM_153758.5:c.-244T>C (IL19) MANE Select | NP_715639.2:n.-244T>C | |
| NR_168466.1:n.361A>G (IL10) |