Linked Data
ClinVar Variation Id:
185444
dbSNP Id:
rs765730332
ExAC:
17:56774107 G / A
gnomAD v2:
17-56774107-G-A
gnomAD v4:
17-58696746-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58696746G>A , CM000679.2:g.58696746G>A | GRCh38 |
| NC_000017.10:g.56774107G>A , CM000679.1:g.56774107G>A | GRCh37 |
| NC_000017.9:g.54129106G>A | NCBI36 |
| NG_023199.1:g.9145G>A , LRG_314:g.9145G>A | |
| NG_047169.1:g.334C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.107G>A | ENSP00000464056.2:p.Gly36Asp | |
| ENST00000697675.1:n.3055G>A | ||
| ENST00000697676.1:n.518G>A | ||
| ENST00000697677.1:n.1539G>A | ||
| ENST00000697678.1:n.360G>A | ||
| ENST00000697679.1:n.1532G>A | ||
| ENST00000697680.1:c.*1322G>A | ENSP00000513392.1:n.*1322G>A | |
| ENST00000697681.1:c.*1349G>A | ENSP00000513393.1:n.*1349G>A | |
| ENST00000697683.1:c.*1322G>A | ENSP00000513395.1:n.*1322G>A | |
| ENST00000697684.1:n.518G>A | ||
| ENST00000697685.1:c.*1268+1557G>A | ENSP00000513396.1:n.*1268+1557G>A | |
| ENST00000697686.1:c.107G>A | ENSP00000513397.1:p.Gly36Asp | |
| ENST00000697687.1:n.450+1557G>A | ||
| ENST00000697688.1:n.504G>A | ||
| ENST00000697689.1:c.*1107+1557G>A | ENSP00000513398.1:n.*1107+1557G>A | |
| ENST00000697690.1:c.458G>A | ENSP00000513399.1:p.Gly153Asp | |
| ENST00000697691.1:c.*430G>A | ENSP00000513400.1:n.*430G>A | |
| ENST00000697692.1:c.*470G>A | ENSP00000513401.1:n.*470G>A | |
| ENST00000697694.1:c.107G>A | ENSP00000513402.1:p.Gly36Asp | |
| ENST00000697695.1:n.1065G>A | ||
| ENST00000337432.9:c.458G>A MANE Select | ENSP00000336701.4:p.Gly153Asp | |
| ENST00000337432.8:c.458G>A | ENSP00000336701.4:p.Gly153Asp | |
| ENST00000413590.5:c.96G>A | ||
| ENST00000425173.5:c.254G>A | ENSP00000407282.1:p.Gly85Asp | |
| ENST00000461271.5:c.107G>A | ENSP00000464056.1:p.Gly36Asp | |
| ENST00000475762.5:c.*1161G>A | ENSP00000432421.1:n.*1161G>A | |
| ENST00000482007.5:c.404+1557G>A | ENSP00000433332.1:n.404+1557G>A | |
| ENST00000487525.5:c.404+1557G>A | ENSP00000431637.1:n.404+1557G>A | |
| ENST00000487921.5:n.370G>A | ||
| ENST00000583539.5:c.458G>A | ENSP00000463121.1:p.Gly153Asp | |
| ENST00000584617.5:c.180G>A | ||
| ENST00000622327.4:c.194G>A | ENSP00000482326.1:p.Gly65Asp | |
| NM_058216.2:c.458G>A | NP_478123.1:p.Gly153Asp | |
| NR_103872.1:n.475+1557G>A | ||
| XM_006722001.2:c.458G>A | XP_006722064.1:p.Gly153Asp | |
| XM_006722002.2:c.458G>A | XP_006722065.1:p.Gly153Asp | |
| XM_006722004.2:c.107G>A | XP_006722067.1:p.Gly36Asp | |
| XM_006722005.2:c.107G>A | XP_006722068.1:p.Gly36Asp | |
| XM_011525092.1:c.107G>A | XP_011523394.1:p.Gly36Asp | |
| XM_011525093.1:c.107G>A | XP_011523395.1:p.Gly36Asp | |
| XM_011525094.1:c.107G>A | XP_011523396.1:p.Gly36Asp | |
| XR_934513.1:n.531G>A | ||
| XR_934514.1:n.531G>A | ||
| XM_006722001.4:c.458G>A | XP_006722064.1:p.Gly153Asp | |
| XM_006722002.4:c.458G>A | XP_006722065.1:p.Gly153Asp | |
| XM_006722004.3:c.107G>A | XP_006722067.1:p.Gly36Asp | |
| XM_006722005.3:c.107G>A | XP_006722068.1:p.Gly36Asp | |
| XM_011525092.2:c.107G>A | XP_011523394.1:p.Gly36Asp | |
| XM_011525093.2:c.107G>A | XP_011523395.1:p.Gly36Asp | |
| XM_011525094.2:c.107G>A | XP_011523396.1:p.Gly36Asp | |
| XM_017024914.1:c.107G>A | XP_016880403.1:p.Gly36Asp | |
| XM_017024915.1:c.107G>A | XP_016880404.1:p.Gly36Asp | |
| XM_017024916.1:c.107G>A | XP_016880405.1:p.Gly36Asp | |
| XM_017024917.1:c.107G>A | XP_016880406.1:p.Gly36Asp | |
| XM_017024918.2:c.107G>A | XP_016880407.1:p.Gly36Asp | |
| XM_017024919.1:c.107G>A | XP_016880408.1:p.Gly36Asp | |
| XR_934513.3:n.962G>A | ||
| XR_934514.3:n.962G>A | ||
| NM_058216.3:c.458G>A MANE Select | NP_478123.1:p.Gly153Asp | |
| NR_103872.2:n.446+1557G>A |