Linked Data
ClinVar Variation Id:
1142522
ClinVar RCV Id:
RCV001480331
dbSNP Id:
rs2140344816
MyVariant Identifiers:
chr15:g.72668263T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72375922T>G , CM000677.2:g.72375922T>G | GRCh38 |
| NC_000015.9:g.72668263T>G , CM000677.1:g.72668263T>G | GRCh37 |
| NC_000015.8:g.70455317T>G | NCBI36 |
| NG_009017.1:g.5258A>C | |
| NG_009017.2:g.5258A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000563908.2:n.64A>C | ||
| ENST00000567027.6:c.51A>C | ENSP00000457521.2:p.Ala17= | |
| ENST00000568260.2:c.51A>C | ENSP00000458128.2:p.Ala17= | |
| ENST00000682061.1:c.51A>C | ENSP00000508316.1:p.Ala17= | |
| ENST00000682177.1:c.51A>C | ENSP00000507409.1:p.Ala17= | |
| ENST00000682461.1:c.51A>C | ENSP00000507308.1:p.Ala17= | |
| ENST00000682653.1:n.82A>C | ||
| ENST00000682657.1:c.51A>C | ENSP00000507753.1:p.Ala17= | |
| ENST00000682721.1:c.51A>C | ENSP00000507535.1:p.Ala17= | |
| ENST00000682843.1:c.51A>C | ENSP00000508173.1:p.Ala17= | |
| ENST00000683003.1:c.51A>C | ENSP00000507576.1:p.Ala17= | |
| ENST00000683133.1:c.51A>C | ENSP00000508108.1:p.Ala17= | |
| ENST00000683228.1:n.82A>C | ||
| ENST00000683243.1:c.51A>C | ENSP00000507042.1:p.Ala17= | |
| ENST00000683463.1:c.51A>C | ENSP00000507986.1:p.Ala17= | |
| ENST00000683548.1:n.82A>C | ||
| ENST00000683579.1:c.51A>C | ENSP00000506867.1:p.Ala17= | |
| ENST00000683587.1:n.82A>C | ||
| ENST00000683681.1:c.51A>C | ENSP00000508110.1:p.Ala17= | |
| ENST00000683735.1:c.51A>C | ENSP00000508336.1:p.Ala17= | |
| ENST00000683853.1:c.51A>C | ENSP00000506834.1:p.Ala17= | |
| ENST00000683860.1:c.51A>C | ENSP00000507179.1:p.Ala17= | |
| ENST00000683884.1:c.51A>C | ENSP00000507004.1:p.Ala17= | |
| ENST00000684041.1:c.51A>C | ENSP00000508382.1:p.Ala17= | |
| ENST00000684125.1:c.51A>C | ENSP00000507320.1:p.Ala17= | |
| ENST00000684203.1:n.68A>C | ||
| ENST00000684231.1:c.51A>C | ENSP00000507748.1:p.Ala17= | |
| ENST00000684263.1:c.51A>C | ENSP00000508369.1:p.Ala17= | |
| ENST00000684305.1:c.51A>C | ENSP00000506819.1:p.Ala17= | |
| ENST00000684415.1:c.51A>C | ENSP00000507227.1:p.Ala17= | |
| ENST00000684520.1:c.51A>C | ENSP00000506826.1:p.Ala17= | |
| ENST00000684602.1:c.51A>C | ENSP00000507996.1:p.Ala17= | |
| ENST00000684667.1:c.51A>C | ENSP00000507003.1:p.Ala17= | |
| ENST00000268097.10:c.51A>C MANE Select | ENSP00000268097.6:p.Ala17= | |
| ENST00000268097.9:c.51A>C | ENSP00000268097.5:p.Ala17= | |
| ENST00000379915.4:c.51A>C | ENSP00000478716.1:p.Ala17= | |
| ENST00000563762.5:c.51A>C | ENSP00000456346.1:p.Ala17= | |
| ENST00000563908.1:n.48A>C | ||
| ENST00000566304.5:c.51A>C | ENSP00000455114.1:p.Ala17= | |
| ENST00000566672.5:c.51A>C | ENSP00000457037.1:p.Ala17= | |
| ENST00000567159.5:c.51A>C | ENSP00000456489.1:p.Ala17= | |
| ENST00000567213.2:c.51A>C | ENSP00000478217.1:p.Ala17= | |
| ENST00000567411.5:c.51A>C | ENSP00000455545.1:p.Ala17= | |
| ENST00000568260.1:c.32A>C | ||
| ENST00000569410.5:c.51A>C | ENSP00000457125.1:p.Ala17= | |
| ENST00000569509.5:n.147-91A>C | ||
| NM_000520.4:c.51A>C | NP_000511.2:p.Ala17= | |
| NM_000520.5:c.51A>C | NP_000511.2:p.Ala17= | |
| NM_001318825.1:c.51A>C | NP_001305754.1:p.Ala17= | |
| NR_134869.1:n.552A>C | ||
| NM_000520.6:c.51A>C MANE Select | NP_000511.2:p.Ala17= | |
| NM_001318825.2:c.51A>C | NP_001305754.1:p.Ala17= | |
| NR_134869.2:n.93A>C | ||
| NR_134869.3:n.93A>C |