Linked Data
ClinVar Variation Id:
300411
dbSNP Id:
rs371967419
ExAC:
10:73450353 C / T
gnomAD v2:
10-73450353-C-T
gnomAD v3:
10-71690596-C-T
gnomAD v4:
10-71690596-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71690596C>T , CM000672.2:g.71690596C>T | GRCh38 |
| NC_000010.10:g.73450353C>T , CM000672.1:g.73450353C>T | GRCh37 |
| NC_000010.9:g.73120359C>T | NCBI36 |
| NG_008835.1:g.298650C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.2176+12C>T MANE Select | ENSP00000224721.9:n.2176+12C>T | |
| ENST00000398809.9:c.2176+12C>T | ENSP00000381789.5:n.2176+12C>T | |
| ENST00000442677.4:c.2176+12C>T | ENSP00000388894.3:n.2176+12C>T | |
| ENST00000466757.8:c.1607+12C>T | ||
| ENST00000224721.10:c.2191+12C>T | ENSP00000224721.8:n.2191+12C>T | |
| ENST00000299366.11:c.2176+12C>T | ENSP00000299366.8:n.2176+12C>T | |
| ENST00000398809.8:c.2176+12C>T | ENSP00000381789.5:n.2176+12C>T | |
| ENST00000442677.3:c.951+12C>T | ||
| ENST00000466757.7:c.1607+12C>T | ||
| ENST00000616684.4:c.2176+12C>T | ENSP00000482036.2:n.2176+12C>T | |
| ENST00000622827.4:c.2176+12C>T | ENSP00000483211.1:n.2176+12C>T | |
| NM_001171930.1:c.2176+12C>T | NP_001165401.1:n.2176+12C>T | |
| NM_001171931.1:c.2176+12C>T | NP_001165402.1:n.2176+12C>T | |
| NM_022124.5:c.2176+12C>T | NP_071407.4:n.2176+12C>T | |
| XM_006717940.2:c.2371+12C>T | XP_006718003.1:n.2371+12C>T | |
| XM_006717942.2:c.2305+12C>T | XP_006718005.1:n.2305+12C>T | |
| XM_011540039.1:c.2371+12C>T | XP_011538341.1:n.2371+12C>T | |
| XM_011540040.1:c.2365+12C>T | XP_011538342.1:n.2365+12C>T | |
| XM_011540041.1:c.2311+12C>T | XP_011538343.1:n.2311+12C>T | |
| XM_011540042.1:c.2371+12C>T | XP_011538344.1:n.2371+12C>T | |
| XM_011540043.1:c.2371+12C>T | XP_011538345.1:n.2371+12C>T | |
| XM_011540044.1:c.2236+12C>T | XP_011538346.1:n.2236+12C>T | |
| XM_011540045.1:c.2371+12C>T | XP_011538347.1:n.2371+12C>T | |
| XM_011540046.1:c.1831+12C>T | XP_011538348.1:n.1831+12C>T | |
| XM_011540047.1:c.1189+12C>T | XP_011538349.1:n.1189+12C>T | |
| XM_011540048.1:c.2371+12C>T | XP_011538350.1:n.2371+12C>T | |
| XM_011540049.1:c.2371+12C>T | XP_011538351.1:n.2371+12C>T | |
| XM_011540050.1:c.2371+12C>T | XP_011538352.1:n.2371+12C>T | |
| XM_011540051.1:c.2371+12C>T | XP_011538353.1:n.2371+12C>T | |
| XM_011540053.1:c.2371+12C>T | XP_011538355.1:n.2371+12C>T | |
| XM_011540054.1:c.2311+12C>T | XP_011538356.1:n.2311+12C>T | |
| XR_945796.1:n.2614+12C>T | ||
| NM_001171930.2:c.2176+12C>T | NP_001165401.1:n.2176+12C>T | |
| NM_001171931.2:c.2176+12C>T | NP_001165402.1:n.2176+12C>T | |
| NM_022124.6:c.2176+12C>T MANE Select | NP_071407.4:n.2176+12C>T |