Linked Data
dbSNP Id:
rs202160996
ExAC:
22:19119265 G / A
gnomAD v2:
22-19119265-G-A
gnomAD v3:
22-19131752-G-A
gnomAD v4:
22-19131752-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19131752G>A , CM000684.2:g.19131752G>A | GRCh38 |
| NC_000022.10:g.19119265G>A , CM000684.1:g.19119265G>A | GRCh37 |
| NC_000022.9:g.17499265G>A | NCBI36 |
| NG_008320.1:g.17926C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252137.11:c.*2444C>T (ESS2) MANE Select | ENSP00000252137.6:n.*2444C>T | |
| ENST00000399635.4:c.353G>A (TSSK2) MANE Select | ENSP00000382544.2:p.Arg118Gln | |
| ENST00000252137.10:c.*2444C>T (ESS2) | ENSP00000252137.6:n.*2444C>T | |
| ENST00000399635.3:c.353G>A (TSSK2) | ENSP00000382544.2:p.Arg118Gln | |
| NM_022719.2:c.*2444C>T (ESS2) | NP_073210.1:n.*2444C>T | |
| NM_053006.4:c.353G>A (TSSK2) | NP_443732.3:p.Arg118Gln | |
| XM_005261282.3:c.*2444C>T (ESS2) | XP_005261339.1:n.*2444C>T | |
| XM_006724329.2:c.*2444C>T (ESS2) | XP_006724392.1:n.*2444C>T | |
| XM_006724330.2:c.*2444C>T (ESS2) | XP_006724393.1:n.*2444C>T | |
| XM_006724331.2:c.*2444C>T (ESS2) | XP_006724394.1:n.*2444C>T | |
| XR_937926.1:n.3833C>T (ESS2) | ||
| NR_134304.1:n.3989C>T (ESS2) | ||
| NM_022719.3:c.*2444C>T (ESS2) MANE Select | NP_073210.1:n.*2444C>T | |
| NM_053006.5:c.353G>A (TSSK2) MANE Select | NP_443732.3:p.Arg118Gln | |
| NR_134304.2:n.3963C>T (ESS2) |