Linked Data
dbSNP Id:
rs754109519
ExAC:
17:79826959 A / C
gnomAD v2:
17-79826959-A-C
gnomAD v4:
17-81869083-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.81869083A>C , CM000679.2:g.81869083A>C | GRCh38 |
| NC_000017.10:g.79826959A>C , CM000679.1:g.79826959A>C | GRCh37 |
| NC_000017.9:g.77420248A>C | NCBI36 |
| NG_034210.1:g.7324T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269321.12:c.416-8T>G MANE Select | ENSP00000269321.7:n.416-8T>G | |
| ENST00000269321.11:c.416-8T>G | ENSP00000269321.7:n.416-8T>G | |
| ENST00000400721.8:c.415+90T>G | ENSP00000383556.4:n.415+90T>G | |
| ENST00000541078.6:c.416-8T>G | ENSP00000441348.2:n.416-8T>G | |
| ENST00000578351.1:c.*60-8T>G | ENSP00000462323.1:n.*60-8T>G | |
| ENST00000579121.5:c.416-8T>G | ENSP00000462960.1:n.416-8T>G | |
| ENST00000580033.5:c.*60-8T>G | ENSP00000463530.1:n.*60-8T>G | |
| ENST00000580685.5:c.416-8T>G | ENSP00000464205.1:n.416-8T>G | |
| ENST00000581876.5:c.191-8T>G | ENSP00000461956.1:n.191-8T>G | |
| ENST00000582984.5:n.618-8T>G | ||
| ENST00000583791.1:n.280-8T>G | ||
| ENST00000583868.5:c.416-8T>G | ENSP00000462209.1:n.416-8T>G | |
| ENST00000584461.5:c.416-8T>G | ENSP00000463939.1:n.416-8T>G | |
| NM_001185077.2:c.416-8T>G | NP_001172006.1:n.416-8T>G | |
| NM_001185078.2:c.415+90T>G | NP_001172007.1:n.415+90T>G | |
| NM_001301240.1:c.416-8T>G | NP_001288169.1:n.416-8T>G | |
| NM_001301241.1:c.416-8T>G | NP_001288170.1:n.416-8T>G | |
| NM_001301242.1:c.416-8T>G | NP_001288171.1:n.416-8T>G | |
| NM_001301243.1:c.551-8T>G | NP_001288172.1:n.551-8T>G | |
| NM_004309.5:c.416-8T>G | NP_004300.1:n.416-8T>G | |
| NR_125441.1:n.475-8T>G | ||
| XM_011523574.1:c.551-8T>G | XP_011521876.1:n.551-8T>G | |
| NM_004309.6:c.416-8T>G MANE Select | NP_004300.1:n.416-8T>G | |
| NM_001185077.3:c.416-8T>G | NP_001172006.1:n.416-8T>G | |
| NM_001185078.3:c.415+90T>G | NP_001172007.1:n.415+90T>G | |
| NM_001301240.2:c.416-8T>G | NP_001288169.1:n.416-8T>G | |
| NM_001301241.2:c.416-8T>G | NP_001288170.1:n.416-8T>G | |
| NM_001301242.2:c.416-8T>G | NP_001288171.1:n.416-8T>G | |
| NM_001301243.2:c.551-8T>G | NP_001288172.1:n.551-8T>G | |
| NR_125441.2:n.406-8T>G |