Linked Data
dbSNP Id:
rs1439898547
gnomAD v2:
7-140481377-A-G
gnomAD v3:
7-140781577-A-G
gnomAD v4:
7-140781577-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140781577A>G , CM000669.2:g.140781577A>G | GRCh38 |
| NC_000007.13:g.140481377A>G , CM000669.1:g.140481377A>G | GRCh37 |
| NC_000007.12:g.140127846A>G | NCBI36 |
| NG_007873.3:g.148188T>C , LRG_299:g.148188T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646891.2:c.1431T>C MANE Select | ENSP00000493543.1:p.His477= | |
| ENST00000288602.11:c.1551T>C | ENSP00000288602.7:p.His517= | |
| ENST00000479537.6:c.101T>C | ||
| ENST00000496384.7:c.1431T>C | ENSP00000419060.2:p.His477= | |
| ENST00000497784.2:c.*881T>C | ENSP00000420119.2:n.*881T>C | |
| ENST00000642228.1:c.*509T>C | ENSP00000493678.1:n.*509T>C | |
| ENST00000642875.1:n.873T>C | ||
| ENST00000644120.1:n.1821T>C | ||
| ENST00000644650.1:c.527T>C | ||
| ENST00000644905.1:n.1520T>C | ||
| ENST00000644969.2:c.1551T>C MANE Plus Clinical | ENSP00000496776.1:p.His517= | |
| ENST00000646334.1:n.561T>C | ||
| ENST00000646730.1:c.1431T>C | ENSP00000494784.1:p.His477= | |
| ENST00000646891.1:c.1431T>C | ENSP00000493543.1:p.His477= | |
| ENST00000647434.1:c.474T>C | ENSP00000495132.1:p.His158= | |
| ENST00000288602.10:c.1431T>C | ENSP00000288602.6:p.His477= | |
| ENST00000496384.6:c.254T>C | ||
| ENST00000497784.1:c.1466T>C | ENSP00000420119.1:n.1466T>C | |
| NM_004333.4:c.1431T>C , LRG_299t1:c.1431T>C | NP_004324.2:p.His477= | |
| XM_005250045.1:c.1431T>C | XP_005250102.1:p.His477= | |
| XM_005250046.1:c.1431T>C | XP_005250103.1:p.His477= | |
| XM_011516529.1:c.1431T>C | XP_011514831.1:p.His477= | |
| XM_011516530.1:c.1431T>C | XP_011514832.1:p.His477= | |
| XR_242190.1:n.1439T>C | ||
| XR_927520.1:n.1439T>C | ||
| XR_927521.1:n.1439T>C | ||
| XR_927522.1:n.1439T>C | ||
| XR_927523.1:n.1439T>C | ||
| NM_001354609.1:c.1431T>C | NP_001341538.1:p.His477= | |
| NM_004333.5:c.1431T>C | NP_004324.2:p.His477= | |
| NR_148928.1:n.1736T>C | ||
| XM_017012558.1:c.1551T>C | XP_016868047.1:p.His517= | |
| XM_017012559.1:c.1551T>C | XP_016868048.1:p.His517= | |
| XR_001744857.1:n.1559T>C | ||
| XR_001744858.1:n.1559T>C | ||
| NM_001354609.2:c.1431T>C | NP_001341538.1:p.His477= | |
| NM_001374244.1:c.1551T>C | NP_001361173.1:p.His517= | |
| NM_001374258.1:c.1551T>C MANE Plus Clinical | NP_001361187.1:p.His517= | |
| NM_004333.6:c.1431T>C MANE Select | NP_004324.2:p.His477= | |
| NM_001378467.1:c.1440T>C | NP_001365396.1:p.His480= | |
| NM_001378468.1:c.1431T>C | NP_001365397.1:p.His477= | |
| NM_001378469.1:c.1365T>C | NP_001365398.1:p.His455= | |
| NM_001378470.1:c.1329T>C | NP_001365399.1:p.His443= | |
| NM_001378471.1:c.1320T>C | NP_001365400.1:p.His440= | |
| NM_001378472.1:c.1275T>C | NP_001365401.1:p.His425= | |
| NM_001378473.1:c.1275T>C | NP_001365402.1:p.His425= | |
| NM_001378474.1:c.1431T>C | NP_001365403.1:p.His477= | |
| NM_001378475.1:c.1167T>C | NP_001365404.1:p.His389= |