Linked Data
dbSNP Id:
rs775468598
ExAC:
22:19119316 G / A
gnomAD v2:
22-19119316-G-A
gnomAD v3:
22-19131803-G-A
gnomAD v4:
22-19131803-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19131803G>A , CM000684.2:g.19131803G>A | GRCh38 |
| NC_000022.10:g.19119316G>A , CM000684.1:g.19119316G>A | GRCh37 |
| NC_000022.9:g.17499316G>A | NCBI36 |
| NG_008320.1:g.17875C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252137.11:c.*2393C>T (ESS2) MANE Select | ENSP00000252137.6:n.*2393C>T | |
| ENST00000399635.4:c.404G>A (TSSK2) MANE Select | ENSP00000382544.2:p.Arg135Gln | |
| ENST00000252137.10:c.*2393C>T (ESS2) | ENSP00000252137.6:n.*2393C>T | |
| ENST00000399635.3:c.404G>A (TSSK2) | ENSP00000382544.2:p.Arg135Gln | |
| NM_022719.2:c.*2393C>T (ESS2) | NP_073210.1:n.*2393C>T | |
| NM_053006.4:c.404G>A (TSSK2) | NP_443732.3:p.Arg135Gln | |
| XM_005261282.3:c.*2393C>T (ESS2) | XP_005261339.1:n.*2393C>T | |
| XM_006724329.2:c.*2393C>T (ESS2) | XP_006724392.1:n.*2393C>T | |
| XM_006724330.2:c.*2393C>T (ESS2) | XP_006724393.1:n.*2393C>T | |
| XM_006724331.2:c.*2393C>T (ESS2) | XP_006724394.1:n.*2393C>T | |
| XR_937926.1:n.3782C>T (ESS2) | ||
| NR_134304.1:n.3938C>T (ESS2) | ||
| NM_022719.3:c.*2393C>T (ESS2) MANE Select | NP_073210.1:n.*2393C>T | |
| NM_053006.5:c.404G>A (TSSK2) MANE Select | NP_443732.3:p.Arg135Gln | |
| NR_134304.2:n.3912C>T (ESS2) |