SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Linked Data
ClinVar Variation Id:
44830
dbSNP Id:
rs397516903
PubMed:
PMID:28135719
ERepo:
CA135140/MONDO:0021060/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140801533A>C , CM000669.2:g.140801533A>C | GRCh38 |
| NC_000007.13:g.140501333A>C , CM000669.1:g.140501333A>C | GRCh37 |
| NC_000007.12:g.140147802A>C | NCBI36 |
| NG_007873.3:g.128232T>G , LRG_299:g.128232T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.739T>G MANE Select | ENSP00000493543.1:p.Phe247Val | |
| ENST00000288602.11:c.739T>G | ENSP00000288602.7:p.Phe247Val | |
| ENST00000496384.7:c.739T>G | ENSP00000419060.2:p.Phe247Val | |
| ENST00000497784.2:c.*189T>G | ENSP00000420119.2:n.*189T>G | |
| ENST00000642228.1:c.739T>G | ENSP00000493678.1:p.Phe247Val | |
| ENST00000642272.1:n.771T>G | ||
| ENST00000642875.1:n.233T>G | ||
| ENST00000643356.1:n.340T>G | ||
| ENST00000644120.1:n.1181T>G | ||
| ENST00000644905.1:n.828T>G | ||
| ENST00000644969.2:c.739T>G MANE Plus Clinical | ENSP00000496776.1:p.Phe247Val | |
| ENST00000646730.1:c.739T>G | ENSP00000494784.1:p.Phe247Val | |
| ENST00000646891.1:c.739T>G | ENSP00000493543.1:p.Phe247Val | |
| ENST00000288602.10:c.739T>G | ENSP00000288602.6:p.Phe247Val | |
| ENST00000497784.1:c.774T>G | ENSP00000420119.1:n.774T>G | |
| NM_004333.4:c.739T>G , LRG_299t1:c.739T>G | NP_004324.2:p.Phe247Val | |
| XM_005250045.1:c.739T>G | XP_005250102.1:p.Phe247Val | |
| XM_005250046.1:c.739T>G | XP_005250103.1:p.Phe247Val | |
| XM_011516529.1:c.739T>G | XP_011514831.1:p.Phe247Val | |
| XM_011516530.1:c.739T>G | XP_011514832.1:p.Phe247Val | |
| XR_242190.1:n.747T>G | ||
| XR_927520.1:n.747T>G | ||
| XR_927521.1:n.747T>G | ||
| XR_927522.1:n.747T>G | ||
| XR_927523.1:n.747T>G | ||
| NM_001354609.1:c.739T>G | NP_001341538.1:p.Phe247Val | |
| NM_004333.5:c.739T>G | NP_004324.2:p.Phe247Val | |
| NR_148928.1:n.1044T>G | ||
| XM_017012558.1:c.739T>G | XP_016868047.1:p.Phe247Val | |
| XM_017012559.1:c.739T>G | XP_016868048.1:p.Phe247Val | |
| XR_001744857.1:n.747T>G | ||
| XR_001744858.1:n.747T>G | ||
| NM_001354609.2:c.739T>G | NP_001341538.1:p.Phe247Val | |
| NM_001374244.1:c.739T>G | NP_001361173.1:p.Phe247Val | |
| NM_001374258.1:c.739T>G MANE Plus Clinical | NP_001361187.1:p.Phe247Val | |
| NM_004333.6:c.739T>G MANE Select | NP_004324.2:p.Phe247Val | |
| NM_001378467.1:c.748T>G | NP_001365396.1:p.Phe250Val | |
| NM_001378468.1:c.739T>G | NP_001365397.1:p.Phe247Val | |
| NM_001378469.1:c.739T>G | NP_001365398.1:p.Phe247Val | |
| NM_001378470.1:c.637T>G | NP_001365399.1:p.Phe213Val | |
| NM_001378471.1:c.739T>G | NP_001365400.1:p.Phe247Val | |
| NM_001378472.1:c.583T>G | NP_001365401.1:p.Phe195Val | |
| NM_001378473.1:c.583T>G | NP_001365402.1:p.Phe195Val | |
| NM_001378474.1:c.739T>G | NP_001365403.1:p.Phe247Val | |
| NM_001378475.1:c.475T>G | NP_001365404.1:p.Phe159Val |