Linked Data
ClinVar Variation Id:
413995
dbSNP Id:
rs139687202
ExAC:
15:44912566 A / G
gnomAD v2:
15-44912566-A-G
gnomAD v3:
15-44620368-A-G
gnomAD v4:
15-44620368-A-G
PubMed:
PMID:18337587
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44620368A>G , CM000677.2:g.44620368A>G | GRCh38 |
| NC_000015.9:g.44912566A>G , CM000677.1:g.44912566A>G | GRCh37 |
| NC_000015.8:g.42699858A>G | NCBI36 |
| NG_008885.1:g.48311T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559511.6:c.2656T>C | ENSP00000453246.2:p.Tyr886His | |
| ENST00000682065.1:c.2656T>C | ENSP00000507025.1:p.Tyr886His | |
| ENST00000682460.1:c.2656T>C | ENSP00000508334.1:p.Tyr886His | |
| ENST00000682495.1:c.2656T>C | ENSP00000507166.1:p.Tyr886His | |
| ENST00000682669.1:c.2656T>C | ENSP00000507782.1:p.Tyr886His | |
| ENST00000682788.1:c.2656T>C | ENSP00000508089.1:p.Tyr886His | |
| ENST00000682915.1:c.2656T>C | ENSP00000507493.1:p.Tyr886His | |
| ENST00000683121.1:c.2656T>C | ENSP00000507557.1:p.Tyr886His | |
| ENST00000683186.1:c.2656T>C | ENSP00000507268.1:p.Tyr886His | |
| ENST00000683255.1:c.2656T>C | ENSP00000508340.1:p.Tyr886His | |
| ENST00000683496.1:c.2656T>C | ENSP00000506968.1:p.Tyr886His | |
| ENST00000683573.1:c.2656T>C | ENSP00000508031.1:p.Tyr886His | |
| ENST00000683734.1:c.2656T>C | ENSP00000508319.1:p.Tyr886His | |
| ENST00000683753.1:n.1780T>C | ||
| ENST00000684038.1:c.2398T>C | ENSP00000507141.1:p.Tyr800His | |
| ENST00000684235.1:c.2656T>C | ENSP00000508295.1:p.Tyr886His | |
| ENST00000684676.1:c.2656T>C | ENSP00000506948.1:p.Tyr886His | |
| ENST00000261866.12:c.2656T>C MANE Select | ENSP00000261866.7:p.Tyr886His | |
| ENST00000261866.11:c.2656T>C | ENSP00000261866.7:p.Tyr886His | |
| ENST00000427534.6:c.2656T>C | ENSP00000396110.2:p.Tyr886His | |
| ENST00000535302.6:c.2656T>C | ENSP00000445278.2:p.Tyr886His | |
| ENST00000558319.5:c.2656T>C | ENSP00000453599.1:p.Tyr886His | |
| ENST00000558989.1:n.1499T>C | ||
| NM_001160227.1:c.2656T>C | NP_001153699.1:p.Tyr886His | |
| NM_025137.3:c.2656T>C | NP_079413.3:p.Tyr886His | |
| XM_005254695.3:c.2398T>C | XP_005254752.1:p.Tyr800His | |
| XM_006720700.1:c.2656T>C | XP_006720763.1:p.Tyr886His | |
| XM_006720701.2:c.2656T>C | XP_006720764.1:p.Tyr886His | |
| XM_011522093.1:c.2656T>C | XP_011520395.1:p.Tyr886His | |
| XR_931917.1:n.2687T>C | ||
| XM_006720701.3:c.2656T>C | XP_006720764.1:p.Tyr886His | |
| XM_017022634.1:c.2656T>C | XP_016878123.1:p.Tyr886His | |
| XM_017022635.2:c.2656T>C | XP_016878124.1:p.Tyr886His | |
| XM_017022636.1:c.-361T>C | XP_016878125.1:n.-361T>C | |
| XR_001751402.1:n.2687T>C | ||
| XR_931917.2:n.2687T>C | ||
| NM_025137.4:c.2656T>C MANE Select | NP_079413.3:p.Tyr886His | |
| NM_001160227.2:c.2656T>C | NP_001153699.1:p.Tyr886His |