Linked Data
ClinVar Variation Id:
180788
ClinVar RCV Id:
RCV000157823
dbSNP Id:
rs397507481
COSMIC:
COSM364756
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140754206G>T , CM000669.2:g.140754206G>T | GRCh38 |
| NC_000007.13:g.140454006G>T , CM000669.1:g.140454006G>T | GRCh37 |
| NC_000007.12:g.140100475G>T | NCBI36 |
| NG_007873.3:g.175559C>A , LRG_299:g.175559C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.1722C>A MANE Select | ENSP00000493543.1:p.His574Gln | |
| ENST00000288602.11:c.1842C>A | ENSP00000288602.7:p.His614Gln | |
| ENST00000479537.6:c.392C>A | ||
| ENST00000496384.7:c.1722C>A | ENSP00000419060.2:p.His574Gln | |
| ENST00000497784.2:c.*1172C>A | ENSP00000420119.2:n.*1172C>A | |
| ENST00000642228.1:c.*800C>A | ENSP00000493678.1:n.*800C>A | |
| ENST00000642875.1:n.1259-4788C>A | ||
| ENST00000644120.1:n.2112C>A | ||
| ENST00000644650.1:c.818C>A | ||
| ENST00000644905.1:n.1811C>A | ||
| ENST00000644969.2:c.1842C>A MANE Plus Clinical | ENSP00000496776.1:p.His614Gln | |
| ENST00000646730.1:c.*298C>A | ENSP00000494784.1:n.*298C>A | |
| ENST00000646891.1:c.1722C>A | ENSP00000493543.1:p.His574Gln | |
| ENST00000647434.1:c.738-4788C>A | ENSP00000495132.1:n.738-4788C>A | |
| ENST00000288602.10:c.1722C>A | ENSP00000288602.6:p.His574Gln | |
| ENST00000479537.5:c.6C>A | ENSP00000418033.1:p.His2Gln | |
| ENST00000496384.6:c.545C>A | ||
| ENST00000497784.1:c.1757C>A | ENSP00000420119.1:n.1757C>A | |
| NM_004333.4:c.1722C>A , LRG_299t1:c.1722C>A | NP_004324.2:p.His574Gln | |
| XM_005250045.1:c.1722C>A | XP_005250102.1:p.His574Gln | |
| XM_005250046.1:c.1722C>A | XP_005250103.1:p.His574Gln | |
| XM_011516529.1:c.1722C>A | XP_011514831.1:p.His574Gln | |
| XM_011516530.1:c.1695-4788C>A | XP_011514832.1:n.1695-4788C>A | |
| XR_242190.1:n.1730C>A | ||
| XR_927520.1:n.1730C>A | ||
| XR_927521.1:n.1730C>A | ||
| XR_927522.1:n.1703-4788C>A | ||
| XR_927523.1:n.1703-4788C>A | ||
| NM_001354609.1:c.1722C>A | NP_001341538.1:p.His574Gln | |
| NM_004333.5:c.1722C>A | NP_004324.2:p.His574Gln | |
| NR_148928.1:n.2027C>A | ||
| XM_017012558.1:c.1842C>A | XP_016868047.1:p.His614Gln | |
| XM_017012559.1:c.1842C>A | XP_016868048.1:p.His614Gln | |
| XR_001744857.1:n.1850C>A | ||
| XR_001744858.1:n.1823-4788C>A | ||
| NM_001354609.2:c.1722C>A | NP_001341538.1:p.His574Gln | |
| NM_001374244.1:c.1842C>A | NP_001361173.1:p.His614Gln | |
| NM_001374258.1:c.1842C>A MANE Plus Clinical | NP_001361187.1:p.His614Gln | |
| NM_004333.6:c.1722C>A MANE Select | NP_004324.2:p.His574Gln | |
| NM_001378467.1:c.1731C>A | NP_001365396.1:p.His577Gln | |
| NM_001378468.1:c.1722C>A | NP_001365397.1:p.His574Gln | |
| NM_001378469.1:c.1656C>A | NP_001365398.1:p.His552Gln | |
| NM_001378470.1:c.1620C>A | NP_001365399.1:p.His540Gln | |
| NM_001378471.1:c.1611C>A | NP_001365400.1:p.His537Gln | |
| NM_001378472.1:c.1566C>A | NP_001365401.1:p.His522Gln | |
| NM_001378473.1:c.1566C>A | NP_001365402.1:p.His522Gln | |
| NM_001378474.1:c.1722C>A | NP_001365403.1:p.His574Gln | |
| NM_001378475.1:c.1458C>A | NP_001365404.1:p.His486Gln |