Linked Data
dbSNP Id:
rs2088604850
gnomAD v4:
15-72345776-T-A
MyVariant Identifiers:
chr15:g.72638117T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72345776T>A , CM000677.2:g.72345776T>A | GRCh38 |
| NC_000015.9:g.72638117T>A , CM000677.1:g.72638117T>A | GRCh37 |
| NC_000015.8:g.70425171T>A | NCBI36 |
| NG_009017.1:g.35404A>T | |
| NG_009017.2:g.35404A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567027.6:c.*82-226A>T | ENSP00000457521.2:n.*82-226A>T | |
| ENST00000682061.1:c.*1542A>T | ENSP00000508316.1:n.*1542A>T | |
| ENST00000682064.1:n.1423A>T | ||
| ENST00000682177.1:c.1465-226A>T | ENSP00000507409.1:n.1465-226A>T | |
| ENST00000682235.1:n.1219A>T | ||
| ENST00000682461.1:c.1528-226A>T | ENSP00000507308.1:n.1528-226A>T | |
| ENST00000682653.1:n.2200A>T | ||
| ENST00000682657.1:c.*1033A>T | ENSP00000507753.1:n.*1033A>T | |
| ENST00000682721.1:c.*1225-226A>T | ENSP00000507535.1:n.*1225-226A>T | |
| ENST00000682843.1:c.*1063-226A>T | ENSP00000508173.1:n.*1063-226A>T | |
| ENST00000683003.1:c.*1033A>T | ENSP00000507576.1:n.*1033A>T | |
| ENST00000683133.1:c.1606-226A>T | ENSP00000508108.1:n.1606-226A>T | |
| ENST00000683243.1:c.*575-226A>T | ENSP00000507042.1:n.*575-226A>T | |
| ENST00000683463.1:c.*685A>T | ENSP00000507986.1:n.*685A>T | |
| ENST00000683548.1:n.1654A>T | ||
| ENST00000683579.1:c.*1320-226A>T | ENSP00000506867.1:n.*1320-226A>T | |
| ENST00000683587.1:n.1727A>T | ||
| ENST00000683681.1:c.1422A>T | ENSP00000508110.1:p.Ter474Cys | |
| ENST00000683735.1:c.*1594A>T | ENSP00000508336.1:n.*1594A>T | |
| ENST00000683853.1:c.*227-226A>T | ENSP00000506834.1:n.*227-226A>T | |
| ENST00000683860.1:c.*316A>T | ENSP00000507179.1:n.*316A>T | |
| ENST00000683884.1:c.*523A>T | ENSP00000507004.1:n.*523A>T | |
| ENST00000684041.1:c.*455A>T | ENSP00000508382.1:n.*455A>T | |
| ENST00000684125.1:c.*82-226A>T | ENSP00000507320.1:n.*82-226A>T | |
| ENST00000684203.1:n.3645A>T | ||
| ENST00000684231.1:c.*832-226A>T | ENSP00000507748.1:n.*832-226A>T | |
| ENST00000684263.1:c.*820A>T | ENSP00000508369.1:n.*820A>T | |
| ENST00000684305.1:c.1870-226A>T | ENSP00000506819.1:n.1870-226A>T | |
| ENST00000684415.1:c.*747A>T | ENSP00000507227.1:n.*747A>T | |
| ENST00000684520.1:c.*455A>T | ENSP00000506826.1:n.*455A>T | |
| ENST00000684602.1:c.*1088-226A>T | ENSP00000507996.1:n.*1088-226A>T | |
| ENST00000684667.1:c.1753-226A>T | ENSP00000507003.1:n.1753-226A>T | |
| ENST00000268097.10:c.1422-226A>T MANE Select | ENSP00000268097.6:n.1422-226A>T | |
| ENST00000268097.9:c.1422-226A>T | ENSP00000268097.5:n.1422-226A>T | |
| ENST00000379915.4:c.504-226A>T | ENSP00000478716.1:n.504-226A>T | |
| ENST00000564677.5:n.114A>T | ||
| ENST00000565873.1:n.107A>T | ||
| ENST00000566304.5:c.1455-226A>T | ENSP00000455114.1:n.1455-226A>T | |
| ENST00000567027.5:c.1037-226A>T | ||
| ENST00000567159.5:c.1422-226A>T | ENSP00000456489.1:n.1422-226A>T | |
| ENST00000567411.5:c.*943-226A>T | ENSP00000455545.1:n.*943-226A>T | |
| ENST00000568777.5:n.6642-226A>T | ||
| ENST00000569116.1:n.29A>T | ||
| NM_000520.4:c.1422-226A>T | NP_000511.2:n.1422-226A>T | |
| NM_000520.5:c.1422-226A>T | NP_000511.2:n.1422-226A>T | |
| NM_001318825.1:c.1455-226A>T | NP_001305754.1:n.1455-226A>T | |
| NR_134869.1:n.1666-226A>T | ||
| NM_000520.6:c.1422-226A>T MANE Select | NP_000511.2:n.1422-226A>T | |
| NM_001318825.2:c.1455-226A>T | NP_001305754.1:n.1455-226A>T | |
| NR_134869.2:n.1207-226A>T | ||
| NR_134869.3:n.1207-226A>T |