Linked Data
ClinVar Variation Id:
283882
dbSNP Id:
rs141046144
ExAC:
16:56534783 G / A
gnomAD v2:
16-56534783-G-A
gnomAD v3:
16-56500871-G-A
gnomAD v4:
16-56500871-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56500871G>A , CM000678.2:g.56500871G>A | GRCh38 |
| NC_000016.9:g.56534783G>A , CM000678.1:g.56534783G>A | GRCh37 |
| NC_000016.8:g.55092284G>A | NCBI36 |
| NG_009312.1:g.24413C>T | |
| NG_009312.2:g.24154C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561877.2:c.1242C>T | ENSP00000454986.2:n.1242C>T | |
| ENST00000562012.2:c.*1209C>T | ENSP00000455651.2:n.*1209C>T | |
| ENST00000562059.2:n.2412C>T | ||
| ENST00000562813.2:n.49C>T | ||
| ENST00000565781.6:n.2756C>T | ||
| ENST00000565859.2:n.2454C>T | ||
| ENST00000566210.2:n.1809C>T | ||
| ENST00000566410.2:n.2739C>T | ||
| ENST00000566495.2:n.349C>T | ||
| ENST00000568104.6:c.1380C>T | ENSP00000456289.1:p.Phe460= | |
| ENST00000569342.6:n.2915C>T | ||
| ENST00000682000.1:n.938C>T | ||
| ENST00000682001.1:n.2409C>T | ||
| ENST00000682005.1:n.1371C>T | ||
| ENST00000682021.1:n.1762C>T | ||
| ENST00000682038.1:c.*644C>T | ENSP00000508404.1:n.*644C>T | |
| ENST00000682047.1:c.1380C>T | ENSP00000507699.1:p.Phe460= | |
| ENST00000682088.1:c.*2166C>T | ENSP00000508064.1:n.*2166C>T | |
| ENST00000682096.1:n.2621C>T | ||
| ENST00000682113.1:n.2388C>T | ||
| ENST00000682146.1:n.2412C>T | ||
| ENST00000682187.1:c.*804C>T | ENSP00000507203.1:n.*804C>T | |
| ENST00000682188.1:c.1380C>T | ENSP00000507655.1:p.Phe460= | |
| ENST00000682201.1:n.1371C>T | ||
| ENST00000682205.1:c.1380C>T | ENSP00000508377.1:p.Phe460= | |
| ENST00000682348.1:c.*429C>T | ENSP00000506965.1:n.*429C>T | |
| ENST00000682360.1:c.783C>T | ENSP00000508007.1:p.Phe261= | |
| ENST00000682370.1:n.2621C>T | ||
| ENST00000682420.1:n.1802C>T | ||
| ENST00000682429.1:c.1225+482C>T | ENSP00000506827.1:n.1225+482C>T | |
| ENST00000682449.1:c.*131C>T | ENSP00000507836.1:n.*131C>T | |
| ENST00000682470.1:c.1380C>T | ENSP00000507654.1:p.Phe460= | |
| ENST00000682473.1:n.1345C>T | ||
| ENST00000682482.1:c.1254C>T | ENSP00000507903.1:p.Phe418= | |
| ENST00000682492.1:n.1485+482C>T | ||
| ENST00000682493.1:c.1380C>T | ENSP00000506778.1:p.Phe460= | |
| ENST00000682543.1:c.*804C>T | ENSP00000507592.1:n.*804C>T | |
| ENST00000682561.1:n.1389C>T | ||
| ENST00000682597.1:n.2621C>T | ||
| ENST00000682658.1:c.*412C>T | ENSP00000507773.1:n.*412C>T | |
| ENST00000682705.1:n.2466+482C>T | ||
| ENST00000682723.1:c.783C>T | ENSP00000507115.1:p.Phe261= | |
| ENST00000682735.1:c.*1839C>T | ENSP00000507007.1:n.*1839C>T | |
| ENST00000682737.1:c.783C>T | ENSP00000506876.1:p.Phe261= | |
| ENST00000682757.1:n.2948C>T | ||
| ENST00000682855.1:c.1380C>T | ENSP00000507027.1:p.Phe460= | |
| ENST00000682857.1:n.1593C>T | ||
| ENST00000682875.1:c.1380C>T | ENSP00000507771.1:p.Phe460= | |
| ENST00000682919.1:n.2842C>T | ||
| ENST00000682930.1:c.1305C>T | ENSP00000507981.1:p.Phe435= | |
| ENST00000682948.1:n.2412C>T | ||
| ENST00000682960.1:n.2412C>T | ||
| ENST00000683008.1:n.2621C>T | ||
| ENST00000683020.1:c.1225+482C>T | ENSP00000507944.1:n.1225+482C>T | |
| ENST00000683099.1:n.2621C>T | ||
| ENST00000683170.1:n.1896C>T | ||
| ENST00000683212.1:c.1225+482C>T | ENSP00000507839.1:n.1225+482C>T | |
| ENST00000683248.1:n.2129C>T | ||
| ENST00000683343.1:n.2251+482C>T | ||
| ENST00000683347.1:n.1587C>T | ||
| ENST00000683384.1:c.1401C>T | ENSP00000508330.1:n.1401C>T | |
| ENST00000683396.1:n.2948C>T | ||
| ENST00000683410.1:n.1802C>T | ||
| ENST00000683443.1:n.1014C>T | ||
| ENST00000683485.1:n.2739C>T | ||
| ENST00000683504.1:n.5762C>T | ||
| ENST00000683533.1:c.*804C>T | ENSP00000508296.1:n.*804C>T | |
| ENST00000683609.1:n.2257+482C>T | ||
| ENST00000683644.1:c.*429C>T | ENSP00000507914.1:n.*429C>T | |
| ENST00000683660.1:n.1593C>T | ||
| ENST00000683669.1:n.1263C>T | ||
| ENST00000683690.1:c.*1623C>T | ENSP00000508152.1:n.*1623C>T | |
| ENST00000683719.1:n.1363C>T | ||
| ENST00000683757.1:n.1369C>T | ||
| ENST00000683858.1:c.1332C>T | ENSP00000507657.1:p.Phe444= | |
| ENST00000683875.1:c.1152C>T | ENSP00000507602.1:p.Phe384= | |
| ENST00000683904.1:n.2739C>T | ||
| ENST00000683910.1:n.1920C>T | ||
| ENST00000683959.1:c.*429C>T | ENSP00000508309.1:n.*429C>T | |
| ENST00000683976.1:c.*929C>T | ENSP00000507183.1:n.*929C>T | |
| ENST00000683978.1:n.1523C>T | ||
| ENST00000683992.1:c.*1020C>T | ENSP00000508144.1:n.*1020C>T | |
| ENST00000684020.1:n.1802C>T | ||
| ENST00000684044.1:n.2257+482C>T | ||
| ENST00000684057.1:n.2170C>T | ||
| ENST00000684076.1:n.1551C>T | ||
| ENST00000684128.1:n.2948C>T | ||
| ENST00000684194.1:n.1802C>T | ||
| ENST00000684205.1:n.3059C>T | ||
| ENST00000684246.1:c.*1020C>T | ENSP00000508273.1:n.*1020C>T | |
| ENST00000684388.1:c.300C>T | ENSP00000507647.1:p.Phe100= | |
| ENST00000684402.1:n.2621C>T | ||
| ENST00000684446.1:n.2739C>T | ||
| ENST00000684531.1:n.1613C>T | ||
| ENST00000684635.1:c.1275C>T | ENSP00000507335.1:p.Phe425= | |
| ENST00000684640.1:c.1231+482C>T | ENSP00000507292.1:n.1231+482C>T | |
| ENST00000684673.1:c.1380C>T | ENSP00000507746.1:p.Phe460= | |
| ENST00000684684.1:c.*649+482C>T | ENSP00000507026.1:n.*649+482C>T | |
| ENST00000245157.11:c.1380C>T MANE Select | ENSP00000245157.5:p.Phe460= | |
| ENST00000245157.9:c.1380C>T | ENSP00000245157.5:p.Phe460= | |
| ENST00000561877.1:c.76C>T | ||
| ENST00000562012.1:c.772C>T | ENSP00000455651.1:n.772C>T | |
| ENST00000562813.1:n.49C>T | ||
| ENST00000565781.5:n.2756C>T | ||
| ENST00000566210.1:n.306C>T | ||
| ENST00000566452.1:n.75C>T | ||
| ENST00000566495.1:n.349C>T | ||
| ENST00000568104.5:c.1380C>T | ENSP00000456289.1:p.Phe460= | |
| NM_031885.3:c.1380C>T | NP_114091.3:p.Phe460= | |
| XM_005256080.1:c.1380C>T | XP_005256137.1:p.Phe460= | |
| XM_005256081.1:c.1380C>T | XP_005256138.1:p.Phe460= | |
| XM_005256082.1:c.1380C>T | XP_005256139.1:p.Phe460= | |
| XR_933378.1:n.1458+482C>T | ||
| XR_933379.1:n.1458+482C>T | ||
| XR_933380.1:n.1458+482C>T | ||
| XM_005256080.2:c.1380C>T | XP_005256137.1:p.Phe460= | |
| XR_001751958.1:n.1613C>T | ||
| XR_001751959.2:n.1613C>T | ||
| XR_001751960.1:n.1458+482C>T | ||
| XR_001751961.1:n.1458+482C>T | ||
| XR_933380.2:n.1458+482C>T | ||
| NM_031885.4:c.1380C>T | NP_114091.3:p.Phe460= | |
| NM_001377456.1:c.1380C>T | NP_001364385.1:p.Phe460= | |
| NM_031885.5:c.1380C>T MANE Select | NP_114091.4:p.Phe460= | |
| NR_165293.1:n.1542C>T | ||
| NR_165294.1:n.1542C>T | ||
| NR_165295.1:n.1387+482C>T | ||
| NR_165296.1:n.1387+482C>T | ||
| NR_165297.1:n.1387+482C>T |