Linked Data
ClinVar Variation Id:
3005032
ClinVar RCV Id:
RCV003861135
dbSNP Id:
rs371497168
ExAC:
7:140476789 G / A
gnomAD v2:
7-140476789-G-A
gnomAD v4:
7-140776989-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140776989G>A , CM000669.2:g.140776989G>A | GRCh38 |
| NC_000007.13:g.140476789G>A , CM000669.1:g.140476789G>A | GRCh37 |
| NC_000007.12:g.140123258G>A | NCBI36 |
| NG_007873.3:g.152776C>T , LRG_299:g.152776C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.1617C>T MANE Select | ENSP00000493543.1:p.His539= | |
| ENST00000288602.11:c.1737C>T | ENSP00000288602.7:p.His579= | |
| ENST00000479537.6:c.287C>T | ||
| ENST00000496384.7:c.1617C>T | ENSP00000419060.2:p.His539= | |
| ENST00000497784.2:c.*1067C>T | ENSP00000420119.2:n.*1067C>T | |
| ENST00000642228.1:c.*695C>T | ENSP00000493678.1:n.*695C>T | |
| ENST00000642875.1:n.1181C>T | ||
| ENST00000644120.1:n.2007C>T | ||
| ENST00000644650.1:c.713C>T | ||
| ENST00000644905.1:n.1706C>T | ||
| ENST00000644969.2:c.1737C>T MANE Plus Clinical | ENSP00000496776.1:p.His579= | |
| ENST00000646730.1:c.1617C>T | ENSP00000494784.1:p.His539= | |
| ENST00000646891.1:c.1617C>T | ENSP00000493543.1:p.His539= | |
| ENST00000647434.1:c.660C>T | ENSP00000495132.1:p.His220= | |
| ENST00000288602.10:c.1617C>T | ENSP00000288602.6:p.His539= | |
| ENST00000496384.6:c.440C>T | ||
| ENST00000497784.1:c.1652C>T | ENSP00000420119.1:n.1652C>T | |
| NM_004333.4:c.1617C>T , LRG_299t1:c.1617C>T | NP_004324.2:p.His539= | |
| XM_005250045.1:c.1617C>T | XP_005250102.1:p.His539= | |
| XM_005250046.1:c.1617C>T | XP_005250103.1:p.His539= | |
| XM_011516529.1:c.1617C>T | XP_011514831.1:p.His539= | |
| XM_011516530.1:c.1617C>T | XP_011514832.1:p.His539= | |
| XR_242190.1:n.1625C>T | ||
| XR_927520.1:n.1625C>T | ||
| XR_927521.1:n.1625C>T | ||
| XR_927522.1:n.1625C>T | ||
| XR_927523.1:n.1625C>T | ||
| NM_001354609.1:c.1617C>T | NP_001341538.1:p.His539= | |
| NM_004333.5:c.1617C>T | NP_004324.2:p.His539= | |
| NR_148928.1:n.1922C>T | ||
| XM_017012558.1:c.1737C>T | XP_016868047.1:p.His579= | |
| XM_017012559.1:c.1737C>T | XP_016868048.1:p.His579= | |
| XR_001744857.1:n.1745C>T | ||
| XR_001744858.1:n.1745C>T | ||
| NM_001354609.2:c.1617C>T | NP_001341538.1:p.His539= | |
| NM_001374244.1:c.1737C>T | NP_001361173.1:p.His579= | |
| NM_001374258.1:c.1737C>T MANE Plus Clinical | NP_001361187.1:p.His579= | |
| NM_004333.6:c.1617C>T MANE Select | NP_004324.2:p.His539= | |
| NM_001378467.1:c.1626C>T | NP_001365396.1:p.His542= | |
| NM_001378468.1:c.1617C>T | NP_001365397.1:p.His539= | |
| NM_001378469.1:c.1551C>T | NP_001365398.1:p.His517= | |
| NM_001378470.1:c.1515C>T | NP_001365399.1:p.His505= | |
| NM_001378471.1:c.1506C>T | NP_001365400.1:p.His502= | |
| NM_001378472.1:c.1461C>T | NP_001365401.1:p.His487= | |
| NM_001378473.1:c.1461C>T | NP_001365402.1:p.His487= | |
| NM_001378474.1:c.1617C>T | NP_001365403.1:p.His539= | |
| NM_001378475.1:c.1353C>T | NP_001365404.1:p.His451= |