Linked Data
dbSNP Id:
rs201382386
ExAC:
11:67250753 C / T
gnomAD v2:
11-67250753-C-T
gnomAD v3:
11-67483282-C-T
gnomAD v4:
11-67483282-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67483282C>T , CM000673.2:g.67483282C>T | GRCh38 |
| NC_000011.9:g.67250753C>T , CM000673.1:g.67250753C>T | GRCh37 |
| NC_000011.8:g.67007329C>T | NCBI36 |
| NG_008969.1:g.5249C>T , LRG_460:g.5249C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525341.2:c.76+25C>T | ||
| ENST00000528641.7:c.99+25C>T | ENSP00000434982.3:n.99+25C>T | |
| ENST00000529797.2:n.29+25C>T | ||
| ENST00000682324.1:c.99+25C>T | ENSP00000508017.1:n.99+25C>T | |
| ENST00000682659.1:c.99+25C>T | ENSP00000507351.1:n.99+25C>T | |
| ENST00000682699.1:c.99+25C>T | ENSP00000507935.1:n.99+25C>T | |
| ENST00000683237.1:c.99+25C>T | ENSP00000507343.1:n.99+25C>T | |
| ENST00000684006.1:c.99+25C>T | ENSP00000507269.1:n.99+25C>T | |
| ENST00000684657.1:c.99+25C>T | ENSP00000507961.1:n.99+25C>T | |
| ENST00000279146.8:c.99+25C>T MANE Select | ENSP00000279146.3:n.99+25C>T | |
| ENST00000279146.7:c.99+25C>T | ENSP00000279146.3:n.99+25C>T | |
| ENST00000528641.6:c.99+25C>T | ENSP00000434982.2:n.99+25C>T | |
| ENST00000529797.1:n.209+25C>T | ||
| NM_001302960.1:c.99+25C>T | NP_001289889.1:n.99+25C>T | |
| NM_003977.3:c.99+25C>T | NP_003968.3:n.99+25C>T | |
| XM_024448761.1:c.99+25C>T | XP_024304529.1:n.99+25C>T | |
| NM_003977.4:c.99+25C>T MANE Select | NP_003968.3:n.99+25C>T | |
| NM_001302960.2:c.99+25C>T | NP_001289889.1:n.99+25C>T |