Linked Data
ClinVar Variation Id:
1005651
ClinVar RCV Id:
RCV001302561
dbSNP Id:
rs150423829
ExAC:
1:206944287 T / A
gnomAD v2:
1-206944287-T-A
gnomAD v3:
1-206770942-T-A
gnomAD v4:
1-206770942-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206770942T>A , CM000663.2:g.206770942T>A | GRCh38 |
| NC_000001.10:g.206944287T>A , CM000663.1:g.206944287T>A | GRCh37 |
| NC_000001.9:g.205010910T>A | NCBI36 |
| NG_012088.1:g.6553A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367099.4:n.248A>T (IL10) | ||
| ENST00000471071.2:c.88A>T (IL10) | ENSP00000493073.2:p.Asn30Tyr | |
| ENST00000659065.2:c.226A>T (IL10) | ENSP00000499588.1:p.Asn76Tyr | |
| ENST00000659642.2:c.226A>T (IL10) | ENSP00000499509.1:p.Asn76Tyr | |
| ENST00000664374.2:c.226A>T (IL10) | ENSP00000499664.1:p.Asn76Tyr | |
| ENST00000659997.3:c.-285T>A (IL19) MANE Select | ENSP00000499459.2:n.-285T>A | |
| ENST00000656872.2:c.-149+112T>A (IL19) | ENSP00000499487.2:n.-149+112T>A | |
| ENST00000659065.1:c.226A>T (IL10) | ENSP00000499588.1:p.Asn76Tyr | |
| ENST00000659642.1:c.226A>T (IL10) | ENSP00000499509.1:p.Asn76Tyr | |
| ENST00000659997.2:c.-285T>A (IL19) | ENSP00000499459.2:n.-285T>A | |
| ENST00000662320.1:n.67+112T>A (IL19) | ||
| ENST00000664374.1:c.226A>T (IL10) | ENSP00000499664.1:p.Asn76Tyr | |
| ENST00000367099.3:n.248A>T (IL10) | ||
| ENST00000423557.1:c.343A>T (IL10) MANE Select | ENSP00000412237.1:p.Asn115Tyr | |
| ENST00000471071.1:n.258A>T (IL10) | ||
| NM_000572.2:c.343A>T (IL10) | NP_000563.1:p.Asn115Tyr | |
| XM_011509506.1:c.343A>T (IL10) | XP_011507808.1:p.Asn115Tyr | |
| NM_000572.3:c.343A>T (IL10) MANE Select | NP_000563.1:p.Asn115Tyr | |
| NM_153758.3:c.-171T>A (IL19) | NP_715639.1:n.-171T>A | |
| NM_001382624.1:c.88A>T (IL10) | NP_001369553.1:p.Asn30Tyr | |
| NM_001393490.1:c.-149+112T>A (IL19) | NP_001380419.1:n.-149+112T>A | |
| NM_153758.5:c.-285T>A (IL19) MANE Select | NP_715639.2:n.-285T>A | |
| NR_168466.1:n.402A>T (IL10) |