Linked Data
ClinVar Variation Id:
1122395
ClinVar RCV Id:
RCV001453059
dbSNP Id:
rs945097885
gnomAD v3:
1-206772352-G-A
gnomAD v4:
1-206772352-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206772352G>A , CM000663.2:g.206772352G>A | GRCh38 |
| NC_000001.10:g.206945697G>A , CM000663.1:g.206945697G>A | GRCh37 |
| NC_000001.9:g.205012320G>A | NCBI36 |
| NG_012088.1:g.5143C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000659065.2:c.-14-20C>T (IL10) | ENSP00000499588.1:n.-14-20C>T | |
| ENST00000659642.2:c.-34C>T (IL10) | ENSP00000499509.1:n.-34C>T | |
| ENST00000664374.2:c.-14-20C>T (IL10) | ENSP00000499664.1:n.-14-20C>T | |
| ENST00000659997.3:c.-149+1274G>A (IL19) MANE Select | ENSP00000499459.2:n.-149+1274G>A | |
| ENST00000656872.2:c.-149+1522G>A (IL19) | ENSP00000499487.2:n.-149+1522G>A | |
| ENST00000659065.1:c.-14-20C>T (IL10) | ENSP00000499588.1:n.-14-20C>T | |
| ENST00000659642.1:c.-34C>T (IL10) | ENSP00000499509.1:n.-34C>T | |
| ENST00000659997.2:c.-149+1274G>A (IL19) | ENSP00000499459.2:n.-149+1274G>A | |
| ENST00000662320.1:n.67+1522G>A (IL19) | ||
| ENST00000664374.1:c.-14-20C>T (IL10) | ENSP00000499664.1:n.-14-20C>T | |
| ENST00000423557.1:c.84C>T (IL10) MANE Select | ENSP00000412237.1:p.Asn28= | |
| NM_000572.2:c.84C>T (IL10) | NP_000563.1:p.Asn28= | |
| XM_011509506.1:c.84C>T (IL10) | XP_011507808.1:p.Asn28= | |
| NM_000572.3:c.84C>T (IL10) MANE Select | NP_000563.1:p.Asn28= | |
| NM_153758.3:c.-35+1274G>A (IL19) | NP_715639.1:n.-35+1274G>A | |
| NM_001393490.1:c.-149+1522G>A (IL19) | NP_001380419.1:n.-149+1522G>A | |
| NM_153758.5:c.-149+1274G>A (IL19) MANE Select | NP_715639.2:n.-149+1274G>A | |
| NR_168466.1:n.143C>T (IL10) |