Linked Data
ClinVar Variation Id:
1151332
ClinVar RCV Id:
RCV001492193
dbSNP Id:
rs2140320704
MyVariant Identifiers:
chr15:g.72638959C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72346618C>T , CM000677.2:g.72346618C>T | GRCh38 |
| NC_000015.9:g.72638959C>T , CM000677.1:g.72638959C>T | GRCh37 |
| NC_000015.8:g.70426013C>T | NCBI36 |
| NG_009017.1:g.34562G>A | |
| NG_009017.2:g.34562G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000567027.6:c.1074-293G>A | ENSP00000457521.2:n.1074-293G>A | |
| ENST00000682061.1:c.*901G>A | ENSP00000508316.1:n.*901G>A | |
| ENST00000682064.1:n.581G>A | ||
| ENST00000682177.1:c.1282G>A | ENSP00000507409.1:n.1282G>A | |
| ENST00000682235.1:n.578G>A | ||
| ENST00000682461.1:c.1345G>A | ENSP00000507308.1:n.1345G>A | |
| ENST00000682653.1:n.1559G>A | ||
| ENST00000682657.1:c.*484-293G>A | ENSP00000507753.1:n.*484-293G>A | |
| ENST00000682721.1:c.*1042G>A | ENSP00000507535.1:n.*1042G>A | |
| ENST00000682843.1:c.*972-293G>A | ENSP00000508173.1:n.*972-293G>A | |
| ENST00000683003.1:c.*484-293G>A | ENSP00000507576.1:n.*484-293G>A | |
| ENST00000683133.1:c.1423G>A | ENSP00000508108.1:n.1423G>A | |
| ENST00000683243.1:c.*484-293G>A | ENSP00000507042.1:n.*484-293G>A | |
| ENST00000683463.1:c.*44G>A | ENSP00000507986.1:n.*44G>A | |
| ENST00000683548.1:n.1105-293G>A | ||
| ENST00000683579.1:c.*1137G>A | ENSP00000506867.1:n.*1137G>A | |
| ENST00000683587.1:n.1178-293G>A | ||
| ENST00000683681.1:c.1239G>A | ENSP00000508110.1:p.Arg413= | |
| ENST00000683735.1:c.*1045-293G>A | ENSP00000508336.1:n.*1045-293G>A | |
| ENST00000683853.1:c.*44G>A | ENSP00000506834.1:n.*44G>A | |
| ENST00000683860.1:c.1239G>A | ENSP00000507179.1:p.Arg413= | |
| ENST00000683884.1:c.1147-293G>A | ENSP00000507004.1:n.1147-293G>A | |
| ENST00000684041.1:c.1239G>A | ENSP00000508382.1:p.Arg413= | |
| ENST00000684125.1:c.1074-293G>A | ENSP00000507320.1:n.1074-293G>A | |
| ENST00000684203.1:n.3004G>A | ||
| ENST00000684231.1:c.*649G>A | ENSP00000507748.1:n.*649G>A | |
| ENST00000684263.1:c.*179G>A | ENSP00000508369.1:n.*179G>A | |
| ENST00000684305.1:c.1687G>A | ENSP00000506819.1:n.1687G>A | |
| ENST00000684415.1:c.*106G>A | ENSP00000507227.1:n.*106G>A | |
| ENST00000684520.1:c.1239G>A | ENSP00000506826.1:p.Arg413= | |
| ENST00000684602.1:c.*905G>A | ENSP00000507996.1:n.*905G>A | |
| ENST00000684667.1:c.1570G>A | ENSP00000507003.1:n.1570G>A | |
| ENST00000268097.10:c.1239G>A MANE Select | ENSP00000268097.6:p.Arg413= | |
| ENST00000268097.9:c.1239G>A | ENSP00000268097.5:p.Arg413= | |
| ENST00000379915.4:c.413-293G>A | ENSP00000478716.1:n.413-293G>A | |
| ENST00000563762.5:c.826-293G>A | ENSP00000456346.1:n.826-293G>A | |
| ENST00000566304.5:c.1272G>A | ENSP00000455114.1:p.Arg424= | |
| ENST00000566672.5:c.*649G>A | ENSP00000457037.1:n.*649G>A | |
| ENST00000567027.5:c.946-293G>A | ||
| ENST00000567159.5:c.1239G>A | ENSP00000456489.1:p.Arg413= | |
| ENST00000567411.5:c.*760G>A | ENSP00000455545.1:n.*760G>A | |
| ENST00000568777.5:n.6551-293G>A | ||
| ENST00000569410.5:c.*44G>A | ENSP00000457125.1:n.*44G>A | |
| NM_000520.4:c.1239G>A | NP_000511.2:p.Arg413= | |
| NM_000520.5:c.1239G>A | NP_000511.2:p.Arg413= | |
| NM_001318825.1:c.1272G>A | NP_001305754.1:p.Arg424= | |
| NR_134869.1:n.1575-293G>A | ||
| NM_000520.6:c.1239G>A MANE Select | NP_000511.2:p.Arg413= | |
| NM_001318825.2:c.1272G>A | NP_001305754.1:p.Arg424= | |
| NR_134869.2:n.1116-293G>A | ||
| NR_134869.3:n.1116-293G>A |