Linked Data
ClinVar Variation Id:
220392
dbSNP Id:
rs147713329
ExAC:
15:44865859 G / C
gnomAD v2:
15-44865859-G-C
gnomAD v3:
15-44573661-G-C
gnomAD v4:
15-44573661-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44573661G>C , CM000677.2:g.44573661G>C | GRCh38 |
| NC_000015.9:g.44865859G>C , CM000677.1:g.44865859G>C | GRCh37 |
| NC_000015.8:g.42653151G>C | NCBI36 |
| NG_008885.1:g.95018C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000559511.6:c.5867-3003C>G | ENSP00000453246.2:n.5867-3003C>G | |
| ENST00000561391.2:n.2319C>G | ||
| ENST00000682065.1:c.5947C>G | ENSP00000507025.1:p.Arg1983Gly | |
| ENST00000682460.1:c.*2348C>G | ENSP00000508334.1:n.*2348C>G | |
| ENST00000682495.1:c.*2583C>G | ENSP00000507166.1:n.*2583C>G | |
| ENST00000682669.1:c.5890C>G | ENSP00000507782.1:p.Arg1964Gly | |
| ENST00000683186.1:c.*2854C>G | ENSP00000507268.1:n.*2854C>G | |
| ENST00000683496.1:c.6006+1241C>G | ENSP00000506968.1:n.6006+1241C>G | |
| ENST00000683734.1:c.*41C>G | ENSP00000508319.1:n.*41C>G | |
| ENST00000683753.1:n.5137C>G | ||
| ENST00000684038.1:c.*2511C>G | ENSP00000507141.1:n.*2511C>G | |
| ENST00000684235.1:c.6091C>G | ENSP00000508295.1:p.Arg2031Gly | |
| ENST00000684676.1:c.*240C>G | ENSP00000506948.1:n.*240C>G | |
| ENST00000261866.12:c.6091C>G MANE Select | ENSP00000261866.7:p.Arg2031Gly | |
| ENST00000261866.11:c.6091C>G | ENSP00000261866.7:p.Arg2031Gly | |
| ENST00000427534.6:c.6091C>G | ENSP00000396110.2:p.Arg2031Gly | |
| ENST00000535302.6:c.5867-841C>G | ENSP00000445278.2:n.5867-841C>G | |
| ENST00000558080.1:n.456C>G | ||
| ENST00000558319.5:c.6091C>G | ENSP00000453599.1:p.Arg2031Gly | |
| ENST00000559511.5:c.715-3003C>G | ||
| ENST00000559933.1:n.160C>G | ||
| ENST00000561268.5:n.23C>G | ||
| NM_001160227.1:c.5867-841C>G | NP_001153699.1:n.5867-841C>G | |
| NM_025137.3:c.6091C>G | NP_079413.3:p.Arg2031Gly | |
| XM_005254695.3:c.5833C>G | XP_005254752.1:p.Arg1945Gly | |
| XM_006720700.1:c.5947C>G | XP_006720763.1:p.Arg1983Gly | |
| XM_017022634.1:c.6091C>G | XP_016878123.1:p.Arg2031Gly | |
| XM_017022636.1:c.2968C>G | XP_016878125.1:p.Arg990Gly | |
| NM_025137.4:c.6091C>G MANE Select | NP_079413.3:p.Arg2031Gly | |
| NM_001160227.2:c.5867-841C>G | NP_001153699.1:n.5867-841C>G |