Linked Data
ClinVar Variation Id:
382758
dbSNP Id:
rs746615745
ExAC:
16:70287677 G / A
gnomAD v2:
16-70287677-G-A
gnomAD v3:
16-70253774-G-A
gnomAD v4:
16-70253774-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.70253774G>A , CM000678.2:g.70253774G>A | GRCh38 |
| NC_000016.9:g.70287677G>A , CM000678.1:g.70287677G>A | GRCh37 |
| NC_000016.8:g.68845178G>A | NCBI36 |
| NG_023191.1:g.40736C>T , LRG_359:g.40736C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261772.13:c.2547C>T MANE Select | ENSP00000261772.8:p.Ile849= | |
| ENST00000565361.3:c.2640C>T | ENSP00000455360.3:p.Ile880= | |
| ENST00000569825.2:n.660C>T | ||
| ENST00000674512.1:c.2526C>T | ENSP00000501613.1:p.Ile842= | |
| ENST00000674652.1:c.*2336C>T | ENSP00000502620.1:n.*2336C>T | |
| ENST00000674691.1:c.2547C>T | ENSP00000502247.1:p.Ile849= | |
| ENST00000674768.1:c.*802C>T | ENSP00000501679.1:n.*802C>T | |
| ENST00000674811.1:c.*740C>T | ENSP00000502055.1:n.*740C>T | |
| ENST00000674848.1:n.2596C>T | ||
| ENST00000674962.1:n.4901C>T | ||
| ENST00000674963.1:c.2547C>T | ENSP00000501924.1:p.Ile849= | |
| ENST00000675035.1:c.*157C>T | ENSP00000502712.1:n.*157C>T | |
| ENST00000675045.1:c.2574C>T | ENSP00000502014.1:p.Ile858= | |
| ENST00000675120.1:c.*857C>T | ENSP00000502823.1:n.*857C>T | |
| ENST00000675133.1:c.2520C>T | ENSP00000502230.1:p.Ile840= | |
| ENST00000675270.1:n.2682C>T | ||
| ENST00000675297.1:c.*1481C>T | ENSP00000502753.1:n.*1481C>T | |
| ENST00000675371.1:c.*157C>T | ENSP00000502645.1:n.*157C>T | |
| ENST00000675403.1:n.3467C>T | ||
| ENST00000675569.1:c.*1781C>T | ENSP00000502534.1:n.*1781C>T | |
| ENST00000675588.1:n.1294C>T | ||
| ENST00000675643.1:c.2547C>T | ENSP00000502797.1:p.Ile849= | |
| ENST00000675691.1:c.2418C>T | ENSP00000502196.1:p.Ile806= | |
| ENST00000675751.1:c.*1574C>T | ENSP00000502277.1:n.*1574C>T | |
| ENST00000675853.1:c.2547C>T | ENSP00000502367.1:p.Ile849= | |
| ENST00000675917.1:n.2844C>T | ||
| ENST00000675953.1:c.2463C>T | ENSP00000502321.1:p.Ile821= | |
| ENST00000675986.1:n.2705C>T | ||
| ENST00000676004.1:c.*2546C>T | ENSP00000502765.1:n.*2546C>T | |
| ENST00000676040.1:c.*1781C>T | ENSP00000502108.1:n.*1781C>T | |
| ENST00000676168.1:c.*157C>T | ENSP00000502479.1:n.*157C>T | |
| ENST00000676209.1:c.*899C>T | ENSP00000502052.1:n.*899C>T | |
| ENST00000676211.1:c.*1574C>T | ENSP00000502726.1:n.*1574C>T | |
| ENST00000676212.1:c.*236C>T | ENSP00000501853.1:n.*236C>T | |
| ENST00000676247.1:c.*899C>T | ENSP00000502699.1:n.*899C>T | |
| ENST00000261772.12:c.2547C>T | ENSP00000261772.7:p.Ile849= | |
| ENST00000569825.1:n.553C>T | ||
| NM_001605.2:c.2547C>T , LRG_359t1:c.2547C>T | NP_001596.2:p.Ile849= | |
| XR_933220.1:n.2513C>T | ||
| XR_933220.3:n.2472C>T | ||
| NM_001605.3:c.2547C>T MANE Select | NP_001596.2:p.Ile849= |