Linked Data
ClinVar Variation Id:
390405
dbSNP Id:
rs184240527
ExAC:
16:70296239 G / A
gnomAD v2:
16-70296239-G-A
gnomAD v3:
16-70262336-G-A
gnomAD v4:
16-70262336-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.70262336G>A , CM000678.2:g.70262336G>A | GRCh38 |
| NC_000016.9:g.70296239G>A , CM000678.1:g.70296239G>A | GRCh37 |
| NC_000016.8:g.68853740G>A | NCBI36 |
| NG_023191.1:g.32174C>T , LRG_359:g.32174C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261772.13:c.1671+10C>T MANE Select | ENSP00000261772.8:n.1671+10C>T | |
| ENST00000564359.6:n.1829+10C>T | ||
| ENST00000565361.3:c.1671+10C>T | ENSP00000455360.3:n.1671+10C>T | |
| ENST00000674512.1:c.1650+31C>T | ENSP00000501613.1:n.1650+31C>T | |
| ENST00000674652.1:c.*698+10C>T | ENSP00000502620.1:n.*698+10C>T | |
| ENST00000674691.1:c.1671+10C>T | ENSP00000502247.1:n.1671+10C>T | |
| ENST00000674768.1:c.1493-1179C>T | ENSP00000501679.1:n.1493-1179C>T | |
| ENST00000674811.1:c.963-3150C>T | ENSP00000502055.1:n.963-3150C>T | |
| ENST00000674848.1:n.1720+10C>T | ||
| ENST00000674962.1:n.1829+10C>T | ||
| ENST00000674963.1:c.1671+10C>T | ENSP00000501924.1:n.1671+10C>T | |
| ENST00000675035.1:c.1671+10C>T | ENSP00000502712.1:n.1671+10C>T | |
| ENST00000675045.1:c.1671+10C>T | ENSP00000502014.1:n.1671+10C>T | |
| ENST00000675120.1:c.1671+10C>T | ENSP00000502823.1:n.1671+10C>T | |
| ENST00000675133.1:c.1644+37C>T | ENSP00000502230.1:n.1644+37C>T | |
| ENST00000675270.1:n.1806+10C>T | ||
| ENST00000675297.1:c.*23+10C>T | ENSP00000502753.1:n.*23+10C>T | |
| ENST00000675371.1:c.1671+10C>T | ENSP00000502645.1:n.1671+10C>T | |
| ENST00000675403.1:n.1829+10C>T | ||
| ENST00000675569.1:c.*905+10C>T | ENSP00000502534.1:n.*905+10C>T | |
| ENST00000675643.1:c.1671+10C>T | ENSP00000502797.1:n.1671+10C>T | |
| ENST00000675691.1:c.1542+10C>T | ENSP00000502196.1:n.1542+10C>T | |
| ENST00000675751.1:c.*698+10C>T | ENSP00000502277.1:n.*698+10C>T | |
| ENST00000675853.1:c.1671+10C>T | ENSP00000502367.1:n.1671+10C>T | |
| ENST00000675917.1:n.1968+10C>T | ||
| ENST00000675953.1:c.1587+10C>T | ENSP00000502321.1:n.1587+10C>T | |
| ENST00000675986.1:n.1829+10C>T | ||
| ENST00000676004.1:c.*1670+10C>T | ENSP00000502765.1:n.*1670+10C>T | |
| ENST00000676040.1:c.*905+10C>T | ENSP00000502108.1:n.*905+10C>T | |
| ENST00000676168.1:c.1671+10C>T | ENSP00000502479.1:n.1671+10C>T | |
| ENST00000676209.1:c.*23+10C>T | ENSP00000502052.1:n.*23+10C>T | |
| ENST00000676211.1:c.*698+10C>T | ENSP00000502726.1:n.*698+10C>T | |
| ENST00000676212.1:c.1671+10C>T | ENSP00000501853.1:n.1671+10C>T | |
| ENST00000676247.1:c.*23+10C>T | ENSP00000502699.1:n.*23+10C>T | |
| ENST00000261772.12:c.1671+10C>T | ENSP00000261772.7:n.1671+10C>T | |
| ENST00000564359.5:n.167+10C>T | ||
| ENST00000565361.2:c.16+10C>T | ||
| ENST00000569790.2:n.264-1179C>T | ||
| NM_001605.2:c.1671+10C>T , LRG_359t1:c.1671+10C>T | NP_001596.2:n.1671+10C>T | |
| XR_933220.1:n.1822+10C>T | ||
| XR_933220.3:n.1781+10C>T | ||
| NM_001605.3:c.1671+10C>T MANE Select | NP_001596.2:n.1671+10C>T |