Linked Data
dbSNP Id:
rs1674904924
gnomAD v3:
1-206773170-GGGGGAAGTGGGTAAGAGTAGT-G
gnomAD v4:
1-206773170-GGGGGAAGTGGGTAAGAGTAGT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206773171_206773191del , CM000663.2:g.206773171_206773191del | GRCh38 |
| NC_000001.10:g.206946516_206946536del , CM000663.1:g.206946516_206946536del | GRCh37 |
| NC_000001.9:g.205013139_205013159del | NCBI36 |
| NG_012088.1:g.4304_4324del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000659065.2:c.-15+489_-15+509del (IL10) | ENSP00000499588.1:n.-15+489_-15+509del | |
| ENST00000659642.2:c.-873_-853del (IL10) | ENSP00000499509.1:n.-873_-853del | |
| ENST00000664374.2:c.-14-859_-14-839del (IL10) | ENSP00000499664.1:n.-14-859_-14-839del | |
| ENST00000659997.3:c.-149+2093_-149+2113del (IL19) MANE Select | ENSP00000499459.2:n.-149+2093_-149+2113del | |
| ENST00000656872.2:c.-149+2341_-149+2361del (IL19) | ENSP00000499487.2:n.-149+2341_-149+2361del | |
| ENST00000659065.1:c.-15+489_-15+509del (IL10) | ENSP00000499588.1:n.-15+489_-15+509del | |
| ENST00000659642.1:c.-873_-853del (IL10) | ENSP00000499509.1:n.-873_-853del | |
| ENST00000659997.2:c.-149+2093_-149+2113del (IL19) | ENSP00000499459.2:n.-149+2093_-149+2113del | |
| ENST00000662320.1:n.67+2341_67+2361del (IL19) | ||
| ENST00000664374.1:c.-14-859_-14-839del (IL10) | ENSP00000499664.1:n.-14-859_-14-839del | |
| XM_011509506.1:c.-756_-736del (IL10) | XP_011507808.1:n.-756_-736del | |
| NM_153758.3:c.-35+2093_-35+2113del (IL19) | NP_715639.1:n.-35+2093_-35+2113del | |
| NM_001393490.1:c.-149+2341_-149+2361del (IL19) | NP_001380419.1:n.-149+2341_-149+2361del | |
| NM_153758.5:c.-149+2093_-149+2113del (IL19) MANE Select | NP_715639.2:n.-149+2093_-149+2113del |