Linked Data
ClinVar Variation Id:
1633412
ClinVar RCV Id:
RCV002121837
dbSNP Id:
rs62487919
gnomAD v2:
7-140481359-C-A
gnomAD v4:
7-140781559-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140781559C>A , CM000669.2:g.140781559C>A | GRCh38 |
| NC_000007.13:g.140481359C>A , CM000669.1:g.140481359C>A | GRCh37 |
| NC_000007.12:g.140127828C>A | NCBI36 |
| NG_007873.3:g.148206G>T , LRG_299:g.148206G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646891.2:c.1432+17G>T MANE Select | ENSP00000493543.1:n.1432+17G>T | |
| ENST00000288602.11:c.1552+17G>T | ENSP00000288602.7:n.1552+17G>T | |
| ENST00000479537.6:c.102+17G>T | ||
| ENST00000496384.7:c.1432+17G>T | ENSP00000419060.2:n.1432+17G>T | |
| ENST00000497784.2:c.*882+17G>T | ENSP00000420119.2:n.*882+17G>T | |
| ENST00000642228.1:c.*510+17G>T | ENSP00000493678.1:n.*510+17G>T | |
| ENST00000642875.1:n.874+17G>T | ||
| ENST00000644120.1:n.1822+17G>T | ||
| ENST00000644650.1:c.528+17G>T | ||
| ENST00000644905.1:n.1521+17G>T | ||
| ENST00000644969.2:c.1552+17G>T MANE Plus Clinical | ENSP00000496776.1:n.1552+17G>T | |
| ENST00000646334.1:n.579G>T | ||
| ENST00000646730.1:c.1432+17G>T | ENSP00000494784.1:n.1432+17G>T | |
| ENST00000646891.1:c.1432+17G>T | ENSP00000493543.1:n.1432+17G>T | |
| ENST00000647434.1:c.475+17G>T | ENSP00000495132.1:n.475+17G>T | |
| ENST00000288602.10:c.1432+17G>T | ENSP00000288602.6:n.1432+17G>T | |
| ENST00000496384.6:c.255+17G>T | ||
| ENST00000497784.1:c.1467+17G>T | ENSP00000420119.1:n.1467+17G>T | |
| NM_004333.4:c.1432+17G>T , LRG_299t1:c.1432+17G>T | NP_004324.2:n.1432+17G>T | |
| XM_005250045.1:c.1432+17G>T | XP_005250102.1:n.1432+17G>T | |
| XM_005250046.1:c.1432+17G>T | XP_005250103.1:n.1432+17G>T | |
| XM_011516529.1:c.1432+17G>T | XP_011514831.1:n.1432+17G>T | |
| XM_011516530.1:c.1432+17G>T | XP_011514832.1:n.1432+17G>T | |
| XR_242190.1:n.1440+17G>T | ||
| XR_927520.1:n.1440+17G>T | ||
| XR_927521.1:n.1440+17G>T | ||
| XR_927522.1:n.1440+17G>T | ||
| XR_927523.1:n.1440+17G>T | ||
| NM_001354609.1:c.1432+17G>T | NP_001341538.1:n.1432+17G>T | |
| NM_004333.5:c.1432+17G>T | NP_004324.2:n.1432+17G>T | |
| NR_148928.1:n.1737+17G>T | ||
| XM_017012558.1:c.1552+17G>T | XP_016868047.1:n.1552+17G>T | |
| XM_017012559.1:c.1552+17G>T | XP_016868048.1:n.1552+17G>T | |
| XR_001744857.1:n.1560+17G>T | ||
| XR_001744858.1:n.1560+17G>T | ||
| NM_001354609.2:c.1432+17G>T | NP_001341538.1:n.1432+17G>T | |
| NM_001374244.1:c.1552+17G>T | NP_001361173.1:n.1552+17G>T | |
| NM_001374258.1:c.1552+17G>T MANE Plus Clinical | NP_001361187.1:n.1552+17G>T | |
| NM_004333.6:c.1432+17G>T MANE Select | NP_004324.2:n.1432+17G>T | |
| NM_001378467.1:c.1441+17G>T | NP_001365396.1:n.1441+17G>T | |
| NM_001378468.1:c.1432+17G>T | NP_001365397.1:n.1432+17G>T | |
| NM_001378469.1:c.1366+17G>T | NP_001365398.1:n.1366+17G>T | |
| NM_001378470.1:c.1330+17G>T | NP_001365399.1:n.1330+17G>T | |
| NM_001378471.1:c.1321+17G>T | NP_001365400.1:n.1321+17G>T | |
| NM_001378472.1:c.1276+17G>T | NP_001365401.1:n.1276+17G>T | |
| NM_001378473.1:c.1276+17G>T | NP_001365402.1:n.1276+17G>T | |
| NM_001378474.1:c.1432+17G>T | NP_001365403.1:n.1432+17G>T | |
| NM_001378475.1:c.1168+17G>T | NP_001365404.1:n.1168+17G>T |