Linked Data
ClinVar Variation Id:
1335459
ClinVar RCV Id:
RCV001816304
dbSNP Id:
rs147456014
ExAC:
20:31024614 G / A
gnomAD v2:
20-31024614-G-A
gnomAD v3:
20-32436811-G-A
gnomAD v4:
20-32436811-G-A
COSMIC:
COSM723114
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.32436811G>A , CM000682.2:g.32436811G>A | GRCh38 |
| NC_000020.10:g.31024614G>A , CM000682.1:g.31024614G>A | GRCh37 |
| NC_000020.9:g.30488275G>A | NCBI36 |
| NG_027868.1:g.83468G>A , LRG_630:g.83468G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375687.10:c.4099G>A MANE Select | ENSP00000364839.4:p.Val1367Ile | |
| ENST00000646985.1:c.3916G>A | ENSP00000495053.1:p.Val1306Ile | |
| ENST00000647223.1:n.6452G>A | ||
| ENST00000651418.1:c.1870-1619G>A | ENSP00000499150.1:n.1870-1619G>A | |
| ENST00000306058.9:c.4084G>A | ENSP00000305119.5:p.Val1362Ile | |
| ENST00000375687.8:c.4099G>A | ENSP00000364839.4:p.Val1367Ile | |
| ENST00000613218.4:c.4099G>A | ENSP00000480487.1:p.Val1367Ile | |
| ENST00000620121.4:c.4099G>A | ENSP00000481978.1:p.Val1367Ile | |
| NM_015338.5:c.4099G>A , LRG_630t1:c.4099G>A | NP_056153.2:p.Val1367Ile | |
| XM_006723727.2:c.4096G>A | XP_006723790.1:p.Val1366Ile | |
| XM_006723728.2:c.4069G>A | XP_006723791.1:p.Val1357Ile | |
| XM_006723730.2:c.4015G>A | XP_006723793.1:p.Val1339Ile | |
| XM_006723732.2:c.3916G>A | XP_006723795.1:p.Val1306Ile | |
| XM_006723733.1:c.3415G>A | XP_006723796.1:p.Val1139Ile | |
| XM_011528647.1:c.4363G>A | XP_011526949.1:p.Val1455Ile | |
| XM_011528648.1:c.4360G>A | XP_011526950.1:p.Val1454Ile | |
| XM_011528649.1:c.4279G>A | XP_011526951.1:p.Val1427Ile | |
| XM_011528650.1:c.4210G>A | XP_011526952.1:p.Val1404Ile | |
| XM_011528651.1:c.4078G>A | XP_011526953.1:p.Val1360Ile | |
| XM_011528652.1:c.4015G>A | XP_011526954.1:p.Val1339Ile | |
| NM_001363734.1:c.3916G>A | NP_001350663.1:p.Val1306Ile | |
| XM_006723727.3:c.4096G>A | XP_006723790.1:p.Val1366Ile | |
| XM_006723728.3:c.4069G>A | XP_006723791.1:p.Val1357Ile | |
| XM_006723730.4:c.4015G>A | XP_006723793.1:p.Val1339Ile | |
| XM_011528648.3:c.4360G>A | XP_011526950.1:p.Val1454Ile | |
| XM_011528652.2:c.4015G>A | XP_011526954.1:p.Val1339Ile | |
| XM_017027704.1:c.4015G>A | XP_016883193.1:p.Val1339Ile | |
| XM_017027705.1:c.4015G>A | XP_016883194.1:p.Val1339Ile | |
| XM_017027706.1:c.3946G>A | XP_016883195.1:p.Val1316Ile | |
| NM_015338.6:c.4099G>A MANE Select | NP_056153.2:p.Val1367Ile |