Linked Data
ClinVar Variation Id:
2120028
ClinVar RCV Id:
RCV003024947
MyVariant Identifiers:
chr11:g.67254602C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67487131C>G , CM000673.2:g.67487131C>G | GRCh38 |
| NC_000011.9:g.67254602C>G , CM000673.1:g.67254602C>G | GRCh37 |
| NC_000011.8:g.67011178C>G | NCBI36 |
| NG_008969.1:g.9098C>G , LRG_460:g.9098C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525341.2:c.202C>G | ||
| ENST00000528641.7:c.225C>G | ENSP00000434982.3:p.Thr75= | |
| ENST00000529797.2:n.155C>G | ||
| ENST00000682324.1:c.225C>G | ENSP00000508017.1:p.Thr75= | |
| ENST00000682659.1:c.100-2907C>G | ENSP00000507351.1:n.100-2907C>G | |
| ENST00000682699.1:c.225C>G | ENSP00000507935.1:p.Thr75= | |
| ENST00000683237.1:c.225C>G | ENSP00000507343.1:p.Thr75= | |
| ENST00000683856.1:c.48C>G | ENSP00000507979.1:p.Thr16= | |
| ENST00000684006.1:c.225C>G | ENSP00000507269.1:p.Thr75= | |
| ENST00000684657.1:c.100-2136C>G | ENSP00000507961.1:n.100-2136C>G | |
| ENST00000279146.8:c.225C>G MANE Select | ENSP00000279146.3:p.Thr75= | |
| ENST00000279146.7:c.225C>G | ENSP00000279146.3:p.Thr75= | |
| ENST00000528641.6:c.225C>G | ENSP00000434982.2:p.Thr75= | |
| ENST00000529797.1:n.335C>G | ||
| NM_001302959.1:c.48C>G | NP_001289888.1:p.Thr16= | |
| NM_001302960.1:c.225C>G | NP_001289889.1:p.Thr75= | |
| NM_003977.3:c.225C>G | NP_003968.3:p.Thr75= | |
| XM_024448761.1:c.225C>G | XP_024304529.1:p.Thr75= | |
| NM_003977.4:c.225C>G MANE Select | NP_003968.3:p.Thr75= | |
| NM_001302960.2:c.225C>G | NP_001289889.1:p.Thr75= | |
| NM_001302959.2:c.48C>G | NP_001289888.1:p.Thr16= |