Linked Data
ClinVar Variation Id:
466533
dbSNP Id:
rs144951661
ExAC:
15:44881601 T / G
gnomAD v2:
15-44881601-T-G
gnomAD v3:
15-44589403-T-G
gnomAD v4:
15-44589403-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44589403T>G , CM000677.2:g.44589403T>G | GRCh38 |
| NC_000015.9:g.44881601T>G , CM000677.1:g.44881601T>G | GRCh37 |
| NC_000015.8:g.42668893T>G | NCBI36 |
| NG_008885.1:g.79276A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559511.6:c.4755A>C | ENSP00000453246.2:p.Ala1585= | |
| ENST00000561391.2:n.983A>C | ||
| ENST00000682065.1:c.4755A>C | ENSP00000507025.1:p.Ala1585= | |
| ENST00000682460.1:c.*1163+2928A>C | ENSP00000508334.1:n.*1163+2928A>C | |
| ENST00000682495.1:c.*1247A>C | ENSP00000507166.1:n.*1247A>C | |
| ENST00000682669.1:c.4554A>C | ENSP00000507782.1:p.Ala1518= | |
| ENST00000682788.1:c.4755A>C | ENSP00000508089.1:p.Ala1585= | |
| ENST00000683121.1:c.*98A>C | ENSP00000507557.1:n.*98A>C | |
| ENST00000683186.1:c.*1518A>C | ENSP00000507268.1:n.*1518A>C | |
| ENST00000683496.1:c.4755A>C | ENSP00000506968.1:p.Ala1585= | |
| ENST00000683734.1:c.4755A>C | ENSP00000508319.1:p.Ala1585= | |
| ENST00000683753.1:n.3801A>C | ||
| ENST00000684038.1:c.*1175A>C | ENSP00000507141.1:n.*1175A>C | |
| ENST00000684235.1:c.4755A>C | ENSP00000508295.1:p.Ala1585= | |
| ENST00000684676.1:c.4755A>C | ENSP00000506948.1:p.Ala1585= | |
| ENST00000261866.12:c.4755A>C MANE Select | ENSP00000261866.7:p.Ala1585= | |
| ENST00000261866.11:c.4755A>C | ENSP00000261866.7:p.Ala1585= | |
| ENST00000427534.6:c.4755A>C | ENSP00000396110.2:p.Ala1585= | |
| ENST00000535302.6:c.4755A>C | ENSP00000445278.2:p.Ala1585= | |
| ENST00000558155.1:c.407A>C | ENSP00000453238.1:n.407A>C | |
| ENST00000558253.5:n.529A>C | ||
| ENST00000558319.5:c.4755A>C | ENSP00000453599.1:p.Ala1585= | |
| ENST00000558790.5:n.120A>C | ||
| ENST00000560858.1:c.135A>C | ENSP00000452991.1:p.Ala45= | |
| NM_001160227.1:c.4755A>C | NP_001153699.1:p.Ala1585= | |
| NM_025137.3:c.4755A>C | NP_079413.3:p.Ala1585= | |
| XM_005254695.3:c.4497A>C | XP_005254752.1:p.Ala1499= | |
| XM_006720700.1:c.4755A>C | XP_006720763.1:p.Ala1585= | |
| XM_006720701.2:c.4743+2928A>C | XP_006720764.1:n.4743+2928A>C | |
| XM_006720701.3:c.4743+2928A>C | XP_006720764.1:n.4743+2928A>C | |
| XM_017022634.1:c.4755A>C | XP_016878123.1:p.Ala1585= | |
| XM_017022636.1:c.1632A>C | XP_016878125.1:p.Ala544= | |
| XR_931917.2:n.4809A>C | ||
| NM_025137.4:c.4755A>C MANE Select | NP_079413.3:p.Ala1585= | |
| NM_001160227.2:c.4755A>C | NP_001153699.1:p.Ala1585= |