Linked Data
ClinVar Variation Id:
6822
dbSNP Id:
rs267606997
ExAC:
17:56787287 G / A
gnomAD v2:
17-56787287-G-A
gnomAD v3:
17-58709926-G-A
gnomAD v4:
17-58709926-G-A
MyVariant Identifiers:
chr17:g.56787287G>A (hg19)
chr17:g.56787287_56787288delinsAT (hg19)
chr17:g.58709926G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58709926G>A , CM000679.2:g.58709926G>A | GRCh38 |
| NC_000017.10:g.56787287G>A , CM000679.1:g.56787287G>A | GRCh37 |
| NC_000017.9:g.54142286G>A | NCBI36 |
| NG_023199.1:g.22325G>A , LRG_314:g.22325G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.422G>A | ENSP00000464056.2:p.Arg141His | |
| ENST00000697678.1:n.675G>A | ||
| ENST00000697679.1:n.1847G>A | ||
| ENST00000697680.1:c.*1637G>A | ENSP00000513392.1:n.*1637G>A | |
| ENST00000697681.1:c.*1934G>A | ENSP00000513393.1:n.*1934G>A | |
| ENST00000697683.1:c.*1637G>A | ENSP00000513395.1:n.*1637G>A | |
| ENST00000697684.1:n.833G>A | ||
| ENST00000697685.1:c.*1470G>A | ENSP00000513396.1:n.*1470G>A | |
| ENST00000697686.1:c.422G>A | ENSP00000513397.1:p.Arg141His | |
| ENST00000697687.1:n.652G>A | ||
| ENST00000697688.1:n.819G>A | ||
| ENST00000697689.1:c.*1309G>A | ENSP00000513398.1:n.*1309G>A | |
| ENST00000697690.1:c.773G>A | ENSP00000513399.1:p.Arg258His | |
| ENST00000697691.1:c.*745G>A | ENSP00000513400.1:n.*745G>A | |
| ENST00000697692.1:c.*785G>A | ENSP00000513401.1:n.*785G>A | |
| ENST00000697694.1:c.422G>A | ENSP00000513402.1:p.Arg141His | |
| ENST00000697695.1:n.1380G>A | ||
| ENST00000337432.9:c.773G>A MANE Select | ENSP00000336701.4:p.Arg258His | |
| ENST00000337432.8:c.773G>A | ENSP00000336701.4:p.Arg258His | |
| ENST00000413590.5:c.411G>A | ||
| ENST00000475762.5:c.*1476G>A | ENSP00000432421.1:n.*1476G>A | |
| ENST00000482007.5:c.*201G>A | ENSP00000433332.1:n.*201G>A | |
| ENST00000487525.5:c.*346G>A | ENSP00000431637.1:n.*346G>A | |
| ENST00000578151.1:n.108G>A | ||
| ENST00000581221.5:n.288G>A | ||
| ENST00000583539.5:c.773G>A | ENSP00000463121.1:p.Arg258His | |
| ENST00000584617.5:c.495G>A | ||
| ENST00000584804.1:c.68G>A | ENSP00000463658.1:p.Arg23His | |
| NM_058216.2:c.773G>A | NP_478123.1:p.Arg258His | |
| NR_103872.1:n.677G>A | ||
| XM_006722001.2:c.773G>A | XP_006722064.1:p.Arg258His | |
| XM_006722002.2:c.773G>A | XP_006722065.1:p.Arg258His | |
| XM_006722004.2:c.422G>A | XP_006722067.1:p.Arg141His | |
| XM_006722005.2:c.422G>A | XP_006722068.1:p.Arg141His | |
| XM_011525092.1:c.422G>A | XP_011523394.1:p.Arg141His | |
| XM_011525093.1:c.422G>A | XP_011523395.1:p.Arg141His | |
| XM_011525094.1:c.422G>A | XP_011523396.1:p.Arg141His | |
| XR_934513.1:n.991G>A | ||
| XR_934514.1:n.991G>A | ||
| XM_006722001.4:c.773G>A | XP_006722064.1:p.Arg258His | |
| XM_006722002.4:c.773G>A | XP_006722065.1:p.Arg258His | |
| XM_006722004.3:c.422G>A | XP_006722067.1:p.Arg141His | |
| XM_006722005.3:c.422G>A | XP_006722068.1:p.Arg141His | |
| XM_011525092.2:c.422G>A | XP_011523394.1:p.Arg141His | |
| XM_011525093.2:c.422G>A | XP_011523395.1:p.Arg141His | |
| XM_011525094.2:c.422G>A | XP_011523396.1:p.Arg141His | |
| XM_017024914.1:c.422G>A | XP_016880403.1:p.Arg141His | |
| XM_017024915.1:c.422G>A | XP_016880404.1:p.Arg141His | |
| XM_017024916.1:c.422G>A | XP_016880405.1:p.Arg141His | |
| XM_017024917.1:c.422G>A | XP_016880406.1:p.Arg141His | |
| XM_017024918.2:c.422G>A | XP_016880407.1:p.Arg141His | |
| XM_017024919.1:c.422G>A | XP_016880408.1:p.Arg141His | |
| XR_934513.3:n.1422G>A | ||
| XR_934514.3:n.1422G>A | ||
| NM_058216.3:c.773G>A MANE Select | NP_478123.1:p.Arg258His | |
| NR_103872.2:n.648G>A |