Linked Data
dbSNP Id:
rs2070788
gnomAD v2:
21-42841988-G-A
gnomAD v3:
21-41470061-G-A
gnomAD v4:
21-41470061-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.41470061G>A , CM000683.2:g.41470061G>A | GRCh38 |
| NC_000021.8:g.42841988G>A , CM000683.1:g.42841988G>A | GRCh37 |
| NC_000021.7:g.41763858G>A | NCBI36 |
| NG_047085.1:g.43098C>T | |
| NG_047085.2:g.66056C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000332149.10:c.1171+587C>T (TMPRSS2) MANE Select | ENSP00000330330.5:n.1171+587C>T | |
| ENST00000424093.6:c.1051+587C>T (TMPRSS2) | ENSP00000397846.2:n.1051+587C>T | |
| ENST00000454499.6:c.1171+587C>T (TMPRSS2) | ENSP00000389006.2:n.1171+587C>T | |
| ENST00000458356.6:c.1171+587C>T (TMPRSS2) | ENSP00000391216.1:n.1171+587C>T | |
| ENST00000676973.1:c.1171+587C>T (TMPRSS2) | ENSP00000504705.1:n.1171+587C>T | |
| ENST00000677680.1:c.*588+587C>T (TMPRSS2) | ENSP00000504526.1:n.*588+587C>T | |
| ENST00000678171.1:c.1171+587C>T (TMPRSS2) | ENSP00000503877.1:n.1171+587C>T | |
| ENST00000678348.1:c.1171+587C>T (TMPRSS2) | ENSP00000503556.1:n.1171+587C>T | |
| ENST00000678617.1:n.1410+587C>T (TMPRSS2) | ||
| ENST00000678743.1:c.847+587C>T (TMPRSS2) | ENSP00000503377.1:n.847+587C>T | |
| ENST00000678959.1:c.*903+587C>T (TMPRSS2) | ENSP00000503114.1:n.*903+587C>T | |
| ENST00000679016.1:c.964+587C>T (TMPRSS2) | ENSP00000504610.1:n.964+587C>T | |
| ENST00000679054.1:c.1171+587C>T (TMPRSS2) | ENSP00000502928.1:n.1171+587C>T | |
| ENST00000679181.1:c.1171+587C>T (TMPRSS2) | ENSP00000504238.1:n.1171+587C>T | |
| ENST00000679263.1:c.1330+587C>T (TMPRSS2) | ENSP00000504602.1:n.1330+587C>T | |
| ENST00000679386.1:c.*1708G>A (MX1) | ENSP00000505700.1:n.*1708G>A | |
| ENST00000332149.9:c.1171+587C>T (TMPRSS2) | ENSP00000330330.5:n.1171+587C>T | |
| ENST00000398585.7:c.1282+587C>T (TMPRSS2) | ENSP00000381588.3:n.1282+587C>T | |
| ENST00000454499.5:c.1171+587C>T (TMPRSS2) | ENSP00000389006.1:n.1171+587C>T | |
| ENST00000458356.5:c.1171+587C>T (TMPRSS2) | ENSP00000391216.1:n.1171+587C>T | |
| NM_001135099.1:c.1282+587C>T (TMPRSS2) | NP_001128571.1:n.1282+587C>T | |
| NM_005656.3:c.1171+587C>T (TMPRSS2) | NP_005647.3:n.1171+587C>T | |
| XM_005261043.2:c.1051+587C>T (TMPRSS2) | XP_005261100.1:n.1051+587C>T | |
| XM_011529731.1:c.1171+587C>T (TMPRSS2) | XP_011528033.1:n.1171+587C>T | |
| XM_011529732.1:c.1171+587C>T (TMPRSS2) | XP_011528034.1:n.1171+587C>T | |
| XM_011529733.1:c.847+587C>T (TMPRSS2) | XP_011528035.1:n.847+587C>T | |
| NM_005656.4:c.1171+587C>T (TMPRSS2) MANE Select | NP_005647.3:n.1171+587C>T | |
| NM_001382720.1:c.1171+587C>T (TMPRSS2) | NP_001369649.1:n.1171+587C>T |