Linked Data
ClinVar Variation Id:
1298449
dbSNP Id:
rs2102439153
MyVariant Identifiers:
chr1:g.206944296G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206770951G>A , CM000663.2:g.206770951G>A | GRCh38 |
| NC_000001.10:g.206944296G>A , CM000663.1:g.206944296G>A | GRCh37 |
| NC_000001.9:g.205010919G>A | NCBI36 |
| NG_012088.1:g.6544C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367099.4:n.239C>T (IL10) | ||
| ENST00000471071.2:c.79C>T (IL10) | ENSP00000493073.2:p.Leu27= | |
| ENST00000659065.2:c.217C>T (IL10) | ENSP00000499588.1:p.Leu73= | |
| ENST00000659642.2:c.217C>T (IL10) | ENSP00000499509.1:p.Leu73= | |
| ENST00000664374.2:c.217C>T (IL10) | ENSP00000499664.1:p.Leu73= | |
| ENST00000659997.3:c.-276G>A (IL19) MANE Select | ENSP00000499459.2:n.-276G>A | |
| ENST00000656872.2:c.-149+121G>A (IL19) | ENSP00000499487.2:n.-149+121G>A | |
| ENST00000659065.1:c.217C>T (IL10) | ENSP00000499588.1:p.Leu73= | |
| ENST00000659642.1:c.217C>T (IL10) | ENSP00000499509.1:p.Leu73= | |
| ENST00000659997.2:c.-276G>A (IL19) | ENSP00000499459.2:n.-276G>A | |
| ENST00000662320.1:n.67+121G>A (IL19) | ||
| ENST00000664374.1:c.217C>T (IL10) | ENSP00000499664.1:p.Leu73= | |
| ENST00000367099.3:n.239C>T (IL10) | ||
| ENST00000423557.1:c.334C>T (IL10) MANE Select | ENSP00000412237.1:p.Leu112= | |
| ENST00000471071.1:n.249C>T (IL10) | ||
| NM_000572.2:c.334C>T (IL10) | NP_000563.1:p.Leu112= | |
| XM_011509506.1:c.334C>T (IL10) | XP_011507808.1:p.Leu112= | |
| NM_000572.3:c.334C>T (IL10) MANE Select | NP_000563.1:p.Leu112= | |
| NM_153758.3:c.-162G>A (IL19) | NP_715639.1:n.-162G>A | |
| NM_001382624.1:c.79C>T (IL10) | NP_001369553.1:p.Leu27= | |
| NM_001393490.1:c.-149+121G>A (IL19) | NP_001380419.1:n.-149+121G>A | |
| NM_153758.5:c.-276G>A (IL19) MANE Select | NP_715639.2:n.-276G>A | |
| NR_168466.1:n.393C>T (IL10) |