Linked Data
ClinVar Variation Id:
128207
ClinVar RCV Id:
RCV000116176
RCV000709506
RCV000206409
RCV000212940
RCV000662721
RCV001356484
RCV004529956
RCV003323404
RCV001798364
dbSNP Id:
rs587780257
gnomAD v2:
17-56774224-A-G
gnomAD v3:
17-58696863-A-G
gnomAD v4:
17-58696863-A-G
PubMed:
PMID:26845104
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58696863A>G , CM000679.2:g.58696863A>G | GRCh38 |
| NC_000017.10:g.56774224A>G , CM000679.1:g.56774224A>G | GRCh37 |
| NC_000017.9:g.54129223A>G | NCBI36 |
| NG_023199.1:g.9262A>G , LRG_314:g.9262A>G | |
| NG_047169.1:g.217T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.220+4A>G | ENSP00000464056.2:n.220+4A>G | |
| ENST00000697675.1:n.3172A>G | ||
| ENST00000697676.1:n.631+4A>G | ||
| ENST00000697677.1:n.1652+4A>G | ||
| ENST00000697678.1:n.473+4A>G | ||
| ENST00000697679.1:n.1645+4A>G | ||
| ENST00000697680.1:c.*1435+4A>G | ENSP00000513392.1:n.*1435+4A>G | |
| ENST00000697681.1:c.*1462+4A>G | ENSP00000513393.1:n.*1462+4A>G | |
| ENST00000697683.1:c.*1435+4A>G | ENSP00000513395.1:n.*1435+4A>G | |
| ENST00000697684.1:n.631+4A>G | ||
| ENST00000697685.1:c.*1268+1674A>G | ENSP00000513396.1:n.*1268+1674A>G | |
| ENST00000697686.1:c.220+4A>G | ENSP00000513397.1:n.220+4A>G | |
| ENST00000697687.1:n.450+1674A>G | ||
| ENST00000697688.1:n.617+4A>G | ||
| ENST00000697689.1:c.*1107+1674A>G | ENSP00000513398.1:n.*1107+1674A>G | |
| ENST00000697690.1:c.571+4A>G | ENSP00000513399.1:n.571+4A>G | |
| ENST00000697691.1:c.*543+4A>G | ENSP00000513400.1:n.*543+4A>G | |
| ENST00000697692.1:c.*583+4A>G | ENSP00000513401.1:n.*583+4A>G | |
| ENST00000697694.1:c.220+4A>G | ENSP00000513402.1:n.220+4A>G | |
| ENST00000697695.1:n.1178+4A>G | ||
| ENST00000337432.9:c.571+4A>G MANE Select | ENSP00000336701.4:n.571+4A>G | |
| ENST00000337432.8:c.571+4A>G | ENSP00000336701.4:n.571+4A>G | |
| ENST00000413590.5:c.209+4A>G | ||
| ENST00000425173.5:c.367+4A>G | ENSP00000407282.1:n.367+4A>G | |
| ENST00000461271.5:c.220+4A>G | ENSP00000464056.1:n.220+4A>G | |
| ENST00000475762.5:c.*1274+4A>G | ENSP00000432421.1:n.*1274+4A>G | |
| ENST00000482007.5:c.404+1674A>G | ENSP00000433332.1:n.404+1674A>G | |
| ENST00000487525.5:c.404+1674A>G | ENSP00000431637.1:n.404+1674A>G | |
| ENST00000487921.5:n.483+4A>G | ||
| ENST00000583539.5:c.571+4A>G | ENSP00000463121.1:n.571+4A>G | |
| ENST00000584617.5:c.293+4A>G | ||
| ENST00000622327.4:c.307+4A>G | ENSP00000482326.1:n.307+4A>G | |
| NM_058216.2:c.571+4A>G | NP_478123.1:n.571+4A>G | |
| NR_103872.1:n.475+1674A>G | ||
| XM_006722001.2:c.571+4A>G | XP_006722064.1:n.571+4A>G | |
| XM_006722002.2:c.571+4A>G | XP_006722065.1:n.571+4A>G | |
| XM_006722004.2:c.220+4A>G | XP_006722067.1:n.220+4A>G | |
| XM_006722005.2:c.220+4A>G | XP_006722068.1:n.220+4A>G | |
| XM_011525092.1:c.220+4A>G | XP_011523394.1:n.220+4A>G | |
| XM_011525093.1:c.220+4A>G | XP_011523395.1:n.220+4A>G | |
| XM_011525094.1:c.220+4A>G | XP_011523396.1:n.220+4A>G | |
| XR_934513.1:n.644+4A>G | ||
| XR_934514.1:n.644+4A>G | ||
| XM_006722001.4:c.571+4A>G | XP_006722064.1:n.571+4A>G | |
| XM_006722002.4:c.571+4A>G | XP_006722065.1:n.571+4A>G | |
| XM_006722004.3:c.220+4A>G | XP_006722067.1:n.220+4A>G | |
| XM_006722005.3:c.220+4A>G | XP_006722068.1:n.220+4A>G | |
| XM_011525092.2:c.220+4A>G | XP_011523394.1:n.220+4A>G | |
| XM_011525093.2:c.220+4A>G | XP_011523395.1:n.220+4A>G | |
| XM_011525094.2:c.220+4A>G | XP_011523396.1:n.220+4A>G | |
| XM_017024914.1:c.220+4A>G | XP_016880403.1:n.220+4A>G | |
| XM_017024915.1:c.220+4A>G | XP_016880404.1:n.220+4A>G | |
| XM_017024916.1:c.220+4A>G | XP_016880405.1:n.220+4A>G | |
| XM_017024917.1:c.220+4A>G | XP_016880406.1:n.220+4A>G | |
| XM_017024918.2:c.220+4A>G | XP_016880407.1:n.220+4A>G | |
| XM_017024919.1:c.220+4A>G | XP_016880408.1:n.220+4A>G | |
| XR_934513.3:n.1075+4A>G | ||
| XR_934514.3:n.1075+4A>G | ||
| NM_058216.3:c.571+4A>G MANE Select | NP_478123.1:n.571+4A>G | |
| NR_103872.2:n.446+1674A>G |