Linked Data
ClinVar Variation Id:
1765024
dbSNP Id:
rs373922286
ExAC:
11:67258360 G / A
gnomAD v2:
11-67258360-G-A
gnomAD v3:
11-67490889-G-A
gnomAD v4:
11-67490889-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67490889G>A , CM000673.2:g.67490889G>A | GRCh38 |
| NC_000011.9:g.67258360G>A , CM000673.1:g.67258360G>A | GRCh37 |
| NC_000011.8:g.67014936G>A | NCBI36 |
| NG_008969.1:g.12856G>A , LRG_460:g.12856G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525341.2:c.1196G>A | ||
| ENST00000528641.7:c.700G>A | ENSP00000434982.3:p.Ala234Thr | |
| ENST00000529797.2:n.1731G>A | ||
| ENST00000682324.1:c.469-108G>A | ENSP00000508017.1:n.469-108G>A | |
| ENST00000682659.1:c.520G>A | ENSP00000507351.1:p.Ala174Thr | |
| ENST00000682699.1:c.889G>A | ENSP00000507935.1:p.Ala297Thr | |
| ENST00000683237.1:c.*29G>A | ENSP00000507343.1:n.*29G>A | |
| ENST00000683856.1:c.712G>A | ENSP00000507979.1:p.Ala238Thr | |
| ENST00000684006.1:c.*29G>A | ENSP00000507269.1:n.*29G>A | |
| ENST00000684657.1:c.709G>A | ENSP00000507961.1:p.Ala237Thr | |
| ENST00000279146.8:c.889G>A MANE Select | ENSP00000279146.3:p.Ala297Thr | |
| ENST00000279146.7:c.889G>A | ENSP00000279146.3:p.Ala297Thr | |
| NM_001302959.1:c.712G>A | NP_001289888.1:p.Ala238Thr | |
| NM_001302960.1:c.*29G>A | NP_001289889.1:n.*29G>A | |
| NM_003977.3:c.889G>A | NP_003968.3:p.Ala297Thr | |
| XM_024448761.1:c.889G>A | XP_024304529.1:p.Ala297Thr | |
| NM_003977.4:c.889G>A MANE Select | NP_003968.3:p.Ala297Thr | |
| NM_001302960.2:c.*29G>A | NP_001289889.1:n.*29G>A | |
| NM_001302959.2:c.712G>A | NP_001289888.1:p.Ala238Thr |