Linked Data
ClinVar Variation Id:
320334
dbSNP Id:
rs777499923
ExAC:
16:70292004 C / G
gnomAD v2:
16-70292004-C-G
gnomAD v3:
16-70258101-C-G
gnomAD v4:
16-70258101-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.70258101C>G , CM000678.2:g.70258101C>G | GRCh38 |
| NC_000016.9:g.70292004C>G , CM000678.1:g.70292004C>G | GRCh37 |
| NC_000016.8:g.68849505C>G | NCBI36 |
| NG_023191.1:g.36409G>C , LRG_359:g.36409G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261772.13:c.2109G>C MANE Select | ENSP00000261772.8:p.Val703= | |
| ENST00000564359.6:n.2150+879G>C | ||
| ENST00000565361.3:c.2109G>C | ENSP00000455360.3:p.Val703= | |
| ENST00000674512.1:c.2088G>C | ENSP00000501613.1:p.Val696= | |
| ENST00000674652.1:c.*1898G>C | ENSP00000502620.1:n.*1898G>C | |
| ENST00000674691.1:c.2109G>C | ENSP00000502247.1:p.Val703= | |
| ENST00000674768.1:c.*364G>C | ENSP00000501679.1:n.*364G>C | |
| ENST00000674811.1:c.*302G>C | ENSP00000502055.1:n.*302G>C | |
| ENST00000674848.1:n.2158G>C | ||
| ENST00000674962.1:n.2267G>C | ||
| ENST00000674963.1:c.2109G>C | ENSP00000501924.1:p.Val703= | |
| ENST00000675035.1:c.2109G>C | ENSP00000502712.1:p.Val703= | |
| ENST00000675045.1:c.2136G>C | ENSP00000502014.1:p.Val712= | |
| ENST00000675120.1:c.*419G>C | ENSP00000502823.1:n.*419G>C | |
| ENST00000675133.1:c.2082G>C | ENSP00000502230.1:p.Val694= | |
| ENST00000675270.1:n.2244G>C | ||
| ENST00000675297.1:c.*461G>C | ENSP00000502753.1:n.*461G>C | |
| ENST00000675371.1:c.1992+879G>C | ENSP00000502645.1:n.1992+879G>C | |
| ENST00000675403.1:n.3029G>C | ||
| ENST00000675569.1:c.*1343G>C | ENSP00000502534.1:n.*1343G>C | |
| ENST00000675643.1:c.2109G>C | ENSP00000502797.1:p.Val703= | |
| ENST00000675691.1:c.1980G>C | ENSP00000502196.1:p.Val660= | |
| ENST00000675751.1:c.*1136G>C | ENSP00000502277.1:n.*1136G>C | |
| ENST00000675853.1:c.2109G>C | ENSP00000502367.1:p.Val703= | |
| ENST00000675917.1:n.2406G>C | ||
| ENST00000675953.1:c.2025G>C | ENSP00000502321.1:p.Val675= | |
| ENST00000675986.1:n.2267G>C | ||
| ENST00000676004.1:c.*2108G>C | ENSP00000502765.1:n.*2108G>C | |
| ENST00000676040.1:c.*1343G>C | ENSP00000502108.1:n.*1343G>C | |
| ENST00000676168.1:c.1992+879G>C | ENSP00000502479.1:n.1992+879G>C | |
| ENST00000676209.1:c.*461G>C | ENSP00000502052.1:n.*461G>C | |
| ENST00000676211.1:c.*1136G>C | ENSP00000502726.1:n.*1136G>C | |
| ENST00000676212.1:c.2109G>C | ENSP00000501853.1:p.Val703= | |
| ENST00000676247.1:c.*461G>C | ENSP00000502699.1:n.*461G>C | |
| ENST00000261772.12:c.2109G>C | ENSP00000261772.7:p.Val703= | |
| ENST00000564359.5:n.488+879G>C | ||
| ENST00000565361.2:c.454G>C | ||
| ENST00000569825.1:n.115G>C | ||
| NM_001605.2:c.2109G>C , LRG_359t1:c.2109G>C | NP_001596.2:p.Val703= | |
| XR_933220.1:n.2143+879G>C | ||
| XR_933220.3:n.2102+879G>C | ||
| NM_001605.3:c.2109G>C MANE Select | NP_001596.2:p.Val703= |