gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.89964405A>G , CM000670.2:g.89964405A>G | GRCh38 |
| NC_000008.10:g.90976633A>G , CM000670.1:g.90976633A>G | GRCh37 |
| NC_000008.9:g.91045809A>G | NCBI36 |
| NG_008860.1:g.25267T>C , LRG_158:g.25267T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494804.2:n.2296+5T>C | ||
| ENST00000517337.2:c.748+5T>C | ENSP00000429971.2:n.748+5T>C | |
| ENST00000523444.2:c.748+5T>C | ENSP00000428252.2:n.748+5T>C | |
| ENST00000697292.1:c.994+5T>C | ENSP00000513229.1:n.994+5T>C | |
| ENST00000697293.1:c.994+5T>C | ENSP00000513230.1:n.994+5T>C | |
| ENST00000697294.1:c.*605+5T>C | ENSP00000513231.1:n.*605+5T>C | |
| ENST00000697295.1:c.*303+5T>C | ENSP00000513232.1:n.*303+5T>C | |
| ENST00000697296.1:c.*662+5T>C | ENSP00000513233.1:n.*662+5T>C | |
| ENST00000697297.1:n.2779+5T>C | ||
| ENST00000697298.1:c.748+5T>C | ENSP00000513234.1:n.748+5T>C | |
| ENST00000697299.1:c.748+5T>C | ENSP00000513235.1:n.748+5T>C | |
| ENST00000697300.1:c.*598+5T>C | ENSP00000513236.1:n.*598+5T>C | |
| ENST00000697301.1:c.*515+5T>C | ENSP00000513237.1:n.*515+5T>C | |
| ENST00000697302.1:c.*515+5T>C | ENSP00000513238.1:n.*515+5T>C | |
| ENST00000697303.1:c.*598+5T>C | ENSP00000513239.1:n.*598+5T>C | |
| ENST00000697304.1:c.682+5T>C | ENSP00000513240.1:n.682+5T>C | |
| ENST00000697306.1:c.481-5551T>C | ENSP00000513241.1:n.481-5551T>C | |
| ENST00000697307.1:c.994+5T>C | ENSP00000513242.1:n.994+5T>C | |
| ENST00000697308.1:c.994+5T>C | ENSP00000513243.1:n.994+5T>C | |
| ENST00000697309.1:c.994+5T>C | ENSP00000513244.1:n.994+5T>C | |
| ENST00000697310.1:c.994+5T>C | ENSP00000513245.1:n.994+5T>C | |
| ENST00000697311.1:c.994+5T>C | ENSP00000513246.1:n.994+5T>C | |
| ENST00000697312.1:c.*392+5T>C | ENSP00000513247.1:n.*392+5T>C | |
| ENST00000697313.1:n.2687+5959T>C | ||
| ENST00000697314.1:n.2785+5T>C | ||
| ENST00000697315.1:c.994+5T>C | ENSP00000513248.1:n.994+5T>C | |
| ENST00000697316.1:n.1115+5T>C | ||
| ENST00000697317.1:n.1104+5T>C | ||
| ENST00000697318.1:n.1106+5T>C | ||
| ENST00000265433.8:c.994+5T>C MANE Select | ENSP00000265433.4:n.994+5T>C | |
| ENST00000265433.7:c.994+5T>C | ENSP00000265433.3:n.994+5T>C | |
| ENST00000396252.6:c.*867+5T>C | ENSP00000379551.2:n.*867+5T>C | |
| ENST00000409330.5:c.748+5T>C | ENSP00000386924.1:n.748+5T>C | |
| NM_001024688.2:c.748+5T>C | NP_001019859.1:n.748+5T>C | |
| NM_002485.4:c.994+5T>C , LRG_158t1:c.994+5T>C | NP_002476.2:n.994+5T>C | |
| XM_011517044.1:c.970+5T>C | XP_011515346.1:n.970+5T>C | |
| XM_011517045.1:c.748+5T>C | XP_011515347.1:n.748+5T>C | |
| XM_011517046.1:c.994+5T>C | XP_011515348.1:n.994+5T>C | |
| XR_928335.1:n.1131+5T>C | ||
| XM_017013460.1:c.115+5T>C | XP_016868949.1:n.115+5T>C | |
| XM_017013462.2:c.115+5T>C | XP_016868951.1:n.115+5T>C | |
| XM_024447163.1:c.748+5T>C | XP_024302931.1:n.748+5T>C | |
| XM_024447164.1:c.748+5T>C | XP_024302932.1:n.748+5T>C | |
| XM_024447165.1:c.115+5T>C | XP_024302933.1:n.115+5T>C | |
| NM_002485.5:c.994+5T>C MANE Select | NP_002476.2:n.994+5T>C | |
| NM_001024688.3:c.748+5T>C | NP_001019859.1:n.748+5T>C |