Linked Data
ClinVar Variation Id:
234385
dbSNP Id:
rs539960851
ExAC:
8:90965929 A / T
gnomAD v2:
8-90965929-A-T
gnomAD v3:
8-89953701-A-T
gnomAD v4:
8-89953701-A-T
COSMIC:
COSM3786052
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.89953701A>T , CM000670.2:g.89953701A>T | GRCh38 |
| NC_000008.10:g.90965929A>T , CM000670.1:g.90965929A>T | GRCh37 |
| NC_000008.9:g.91035105A>T | NCBI36 |
| NG_008860.1:g.35971T>A , LRG_158:g.35971T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494804.2:n.2700-10T>A | ||
| ENST00000517337.2:c.1152-10T>A | ENSP00000429971.2:n.1152-10T>A | |
| ENST00000523444.2:c.1152-10T>A | ENSP00000428252.2:n.1152-10T>A | |
| ENST00000697292.1:c.1398-10T>A | ENSP00000513229.1:n.1398-10T>A | |
| ENST00000697293.1:c.1398-10T>A | ENSP00000513230.1:n.1398-10T>A | |
| ENST00000697294.1:c.*1009-10T>A | ENSP00000513231.1:n.*1009-10T>A | |
| ENST00000697295.1:c.*707-10T>A | ENSP00000513232.1:n.*707-10T>A | |
| ENST00000697296.1:c.*1066-10T>A | ENSP00000513233.1:n.*1066-10T>A | |
| ENST00000697297.1:n.3183-10T>A | ||
| ENST00000697298.1:c.1152-10T>A | ENSP00000513234.1:n.1152-10T>A | |
| ENST00000697299.1:c.1152-10T>A | ENSP00000513235.1:n.1152-10T>A | |
| ENST00000697300.1:c.*1002-10T>A | ENSP00000513236.1:n.*1002-10T>A | |
| ENST00000697301.1:c.*919-10T>A | ENSP00000513237.1:n.*919-10T>A | |
| ENST00000697302.1:c.*919-10T>A | ENSP00000513238.1:n.*919-10T>A | |
| ENST00000697303.1:c.*1002-10T>A | ENSP00000513239.1:n.*1002-10T>A | |
| ENST00000697304.1:c.1086-10T>A | ENSP00000513240.1:n.1086-10T>A | |
| ENST00000697306.1:c.*398-10T>A | ENSP00000513241.1:n.*398-10T>A | |
| ENST00000697307.1:c.1398-10T>A | ENSP00000513242.1:n.1398-10T>A | |
| ENST00000697308.1:c.1398-10T>A | ENSP00000513243.1:n.1398-10T>A | |
| ENST00000697309.1:c.1398-10T>A | ENSP00000513244.1:n.1398-10T>A | |
| ENST00000697310.1:c.1398-10T>A | ENSP00000513245.1:n.1398-10T>A | |
| ENST00000697311.1:c.1398-10T>A | ENSP00000513246.1:n.1398-10T>A | |
| ENST00000697312.1:c.*796-10T>A | ENSP00000513247.1:n.*796-10T>A | |
| ENST00000697313.1:n.2687+16663T>A | ||
| ENST00000697314.1:n.3189-10T>A | ||
| ENST00000697315.1:c.1398-10T>A | ENSP00000513248.1:n.1398-10T>A | |
| ENST00000697316.1:n.1519-10T>A | ||
| ENST00000697317.1:n.1508-10T>A | ||
| ENST00000697318.1:n.1510-10T>A | ||
| ENST00000265433.8:c.1398-10T>A MANE Select | ENSP00000265433.4:n.1398-10T>A | |
| ENST00000265433.7:c.1398-10T>A | ENSP00000265433.3:n.1398-10T>A | |
| ENST00000396252.6:c.*1271-10T>A | ENSP00000379551.2:n.*1271-10T>A | |
| ENST00000409330.5:c.1152-10T>A | ENSP00000386924.1:n.1152-10T>A | |
| NM_001024688.2:c.1152-10T>A | NP_001019859.1:n.1152-10T>A | |
| NM_002485.4:c.1398-10T>A , LRG_158t1:c.1398-10T>A | NP_002476.2:n.1398-10T>A | |
| XM_011517044.1:c.1374-10T>A | XP_011515346.1:n.1374-10T>A | |
| XM_011517045.1:c.1152-10T>A | XP_011515347.1:n.1152-10T>A | |
| XM_011517046.1:c.1396-7T>A | XP_011515348.1:n.1396-7T>A | |
| XR_928335.1:n.1534-7T>A | ||
| XM_017013460.1:c.519-10T>A | XP_016868949.1:n.519-10T>A | |
| XM_017013462.2:c.519-10T>A | XP_016868951.1:n.519-10T>A | |
| XM_024447163.1:c.1152-10T>A | XP_024302931.1:n.1152-10T>A | |
| XM_024447164.1:c.1152-10T>A | XP_024302932.1:n.1152-10T>A | |
| XM_024447165.1:c.519-10T>A | XP_024302933.1:n.519-10T>A | |
| NM_002485.5:c.1398-10T>A MANE Select | NP_002476.2:n.1398-10T>A | |
| NM_001024688.3:c.1152-10T>A | NP_001019859.1:n.1152-10T>A |