Linked Data
dbSNP Id:
rs1800893
gnomAD v2:
1-206947167-C-T
gnomAD v3:
1-206773822-C-T
gnomAD v4:
1-206773822-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206773822C>T , CM000663.2:g.206773822C>T | GRCh38 |
| NC_000001.10:g.206947167C>T , CM000663.1:g.206947167C>T | GRCh37 |
| NC_000001.9:g.205013790C>T | NCBI36 |
| NG_012088.1:g.3673G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000659065.2:c.-144-13G>A (IL10) | ENSP00000499588.1:n.-144-13G>A | |
| ENST00000659642.2:c.-1118-386G>A (IL10) | ENSP00000499509.1:n.-1118-386G>A | |
| ENST00000664374.2:c.-15+508G>A (IL10) | ENSP00000499664.1:n.-15+508G>A | |
| ENST00000659997.3:c.-149+2744C>T (IL19) MANE Select | ENSP00000499459.2:n.-149+2744C>T | |
| ENST00000656872.2:c.-149+2992C>T (IL19) | ENSP00000499487.2:n.-149+2992C>T | |
| ENST00000659065.1:c.-144-13G>A (IL10) | ENSP00000499588.1:n.-144-13G>A | |
| ENST00000659642.1:c.-1118-386G>A (IL10) | ENSP00000499509.1:n.-1118-386G>A | |
| ENST00000659997.2:c.-149+2744C>T (IL19) | ENSP00000499459.2:n.-149+2744C>T | |
| ENST00000662320.1:n.67+2992C>T (IL19) | ||
| ENST00000664374.1:c.-15+508G>A (IL10) | ENSP00000499664.1:n.-15+508G>A | |
| XM_011509506.1:c.-1001-386G>A (IL10) | XP_011507808.1:n.-1001-386G>A | |
| NM_153758.3:c.-35+2744C>T (IL19) | NP_715639.1:n.-35+2744C>T | |
| NM_001393490.1:c.-149+2992C>T (IL19) | NP_001380419.1:n.-149+2992C>T | |
| NM_153758.5:c.-149+2744C>T (IL19) MANE Select | NP_715639.2:n.-149+2744C>T |