Linked Data
ClinVar Variation Id:
981545
ClinVar RCV Id:
RCV001261048
dbSNP Id:
rs1586018613
MyVariant Identifiers:
chr7:g.140453988A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140754188A>G , CM000669.2:g.140754188A>G | GRCh38 |
| NC_000007.13:g.140453988A>G , CM000669.1:g.140453988A>G | GRCh37 |
| NC_000007.12:g.140100457A>G | NCBI36 |
| NG_007873.3:g.175577T>C , LRG_299:g.175577T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646891.2:c.1740T>C MANE Select | ENSP00000493543.1:p.Asn580= | |
| ENST00000288602.11:c.1860T>C | ENSP00000288602.7:p.Asn620= | |
| ENST00000479537.6:c.410T>C | ||
| ENST00000496384.7:c.1740T>C | ENSP00000419060.2:p.Asn580= | |
| ENST00000497784.2:c.*1190T>C | ENSP00000420119.2:n.*1190T>C | |
| ENST00000642228.1:c.*818T>C | ENSP00000493678.1:n.*818T>C | |
| ENST00000642875.1:n.1259-4770T>C | ||
| ENST00000644120.1:n.2130T>C | ||
| ENST00000644650.1:c.836T>C | ||
| ENST00000644905.1:n.1829T>C | ||
| ENST00000644969.2:c.1860T>C MANE Plus Clinical | ENSP00000496776.1:p.Asn620= | |
| ENST00000646730.1:c.*316T>C | ENSP00000494784.1:n.*316T>C | |
| ENST00000646891.1:c.1740T>C | ENSP00000493543.1:p.Asn580= | |
| ENST00000647434.1:c.738-4770T>C | ENSP00000495132.1:n.738-4770T>C | |
| ENST00000288602.10:c.1740T>C | ENSP00000288602.6:p.Asn580= | |
| ENST00000479537.5:c.24T>C | ENSP00000418033.1:p.Asn8= | |
| ENST00000496384.6:c.563T>C | ||
| ENST00000497784.1:c.1775T>C | ENSP00000420119.1:n.1775T>C | |
| NM_004333.4:c.1740T>C , LRG_299t1:c.1740T>C | NP_004324.2:p.Asn580= | |
| XM_005250045.1:c.1740T>C | XP_005250102.1:p.Asn580= | |
| XM_005250046.1:c.1740T>C | XP_005250103.1:p.Asn580= | |
| XM_011516529.1:c.1740T>C | XP_011514831.1:p.Asn580= | |
| XM_011516530.1:c.1695-4770T>C | XP_011514832.1:n.1695-4770T>C | |
| XR_242190.1:n.1748T>C | ||
| XR_927520.1:n.1748T>C | ||
| XR_927521.1:n.1748T>C | ||
| XR_927522.1:n.1703-4770T>C | ||
| XR_927523.1:n.1703-4770T>C | ||
| NM_001354609.1:c.1740T>C | NP_001341538.1:p.Asn580= | |
| NM_004333.5:c.1740T>C | NP_004324.2:p.Asn580= | |
| NR_148928.1:n.2045T>C | ||
| XM_017012558.1:c.1860T>C | XP_016868047.1:p.Asn620= | |
| XM_017012559.1:c.1860T>C | XP_016868048.1:p.Asn620= | |
| XR_001744857.1:n.1868T>C | ||
| XR_001744858.1:n.1823-4770T>C | ||
| NM_001354609.2:c.1740T>C | NP_001341538.1:p.Asn580= | |
| NM_001374244.1:c.1860T>C | NP_001361173.1:p.Asn620= | |
| NM_001374258.1:c.1860T>C MANE Plus Clinical | NP_001361187.1:p.Asn620= | |
| NM_004333.6:c.1740T>C MANE Select | NP_004324.2:p.Asn580= | |
| NM_001378467.1:c.1749T>C | NP_001365396.1:p.Asn583= | |
| NM_001378468.1:c.1740T>C | NP_001365397.1:p.Asn580= | |
| NM_001378469.1:c.1674T>C | NP_001365398.1:p.Asn558= | |
| NM_001378470.1:c.1638T>C | NP_001365399.1:p.Asn546= | |
| NM_001378471.1:c.1629T>C | NP_001365400.1:p.Asn543= | |
| NM_001378472.1:c.1584T>C | NP_001365401.1:p.Asn528= | |
| NM_001378473.1:c.1584T>C | NP_001365402.1:p.Asn528= | |
| NM_001378474.1:c.1740T>C | NP_001365403.1:p.Asn580= | |
| NM_001378475.1:c.1476T>C | NP_001365404.1:p.Asn492= |