Linked Data
dbSNP Id:
rs762750138
ExAC:
1:206944381 C / A
gnomAD v2:
1-206944381-C-A
gnomAD v3:
1-206771036-C-A
gnomAD v4:
1-206771036-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206771036C>A , CM000663.2:g.206771036C>A | GRCh38 |
| NC_000001.10:g.206944381C>A , CM000663.1:g.206944381C>A | GRCh37 |
| NC_000001.9:g.205011004C>A | NCBI36 |
| NG_012088.1:g.6459G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367099.4:n.154G>T (IL10) | ||
| ENST00000471071.2:c.-7G>T (IL10) | ENSP00000493073.2:n.-7G>T | |
| ENST00000659065.2:c.132G>T (IL10) | ENSP00000499588.1:p.Leu44Phe | |
| ENST00000659642.2:c.132G>T (IL10) | ENSP00000499509.1:p.Leu44Phe | |
| ENST00000664374.2:c.132G>T (IL10) | ENSP00000499664.1:p.Leu44Phe | |
| ENST00000659997.3:c.-191C>A (IL19) MANE Select | ENSP00000499459.2:n.-191C>A | |
| ENST00000656872.2:c.-149+206C>A (IL19) | ENSP00000499487.2:n.-149+206C>A | |
| ENST00000659065.1:c.132G>T (IL10) | ENSP00000499588.1:p.Leu44Phe | |
| ENST00000659642.1:c.132G>T (IL10) | ENSP00000499509.1:p.Leu44Phe | |
| ENST00000659997.2:c.-191C>A (IL19) | ENSP00000499459.2:n.-191C>A | |
| ENST00000662320.1:n.67+206C>A (IL19) | ||
| ENST00000664374.1:c.132G>T (IL10) | ENSP00000499664.1:p.Leu44Phe | |
| ENST00000367099.3:n.154G>T (IL10) | ||
| ENST00000423557.1:c.249G>T (IL10) MANE Select | ENSP00000412237.1:p.Leu83Phe | |
| ENST00000471071.1:n.164G>T (IL10) | ||
| NM_000572.2:c.249G>T (IL10) | NP_000563.1:p.Leu83Phe | |
| XM_011509506.1:c.249G>T (IL10) | XP_011507808.1:p.Leu83Phe | |
| NM_000572.3:c.249G>T (IL10) MANE Select | NP_000563.1:p.Leu83Phe | |
| NM_153758.3:c.-77C>A (IL19) | NP_715639.1:n.-77C>A | |
| NM_001382624.1:c.-7G>T (IL10) | NP_001369553.1:n.-7G>T | |
| NM_001393490.1:c.-149+206C>A (IL19) | NP_001380419.1:n.-149+206C>A | |
| NM_153758.5:c.-191C>A (IL19) MANE Select | NP_715639.2:n.-191C>A | |
| NR_168466.1:n.308G>T (IL10) |