Linked Data
ClinVar Variation Id:
233608
dbSNP Id:
rs876660519
gnomAD v2:
17-59858236-G-C
gnomAD v3:
17-61780875-G-C
gnomAD v4:
17-61780875-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61780875G>C , CM000679.2:g.61780875G>C | GRCh38 |
| NC_000017.10:g.59858236G>C , CM000679.1:g.59858236G>C | GRCh37 |
| NC_000017.9:g.57213018G>C | NCBI36 |
| NG_007409.2:g.87685C>G , LRG_300:g.87685C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000579028.2:c.1341C>G | ENSP00000463827.2:n.1341C>G | |
| ENST00000584322.2:c.1759C>G | ENSP00000463272.2:p.His587Asp | |
| ENST00000682066.1:c.1252C>G | ENSP00000507191.1:p.His418Asp | |
| ENST00000682073.1:n.499C>G | ||
| ENST00000682453.1:c.1759C>G | ENSP00000506943.1:p.His587Asp | |
| ENST00000682477.1:c.*1185C>G | ENSP00000507075.1:n.*1185C>G | |
| ENST00000682589.1:n.3500C>G | ||
| ENST00000682611.1:c.1252C>G | ENSP00000508326.1:p.His418Asp | |
| ENST00000682755.1:c.1537C>G | ENSP00000507660.1:p.His513Asp | |
| ENST00000682989.1:c.1759C>G | ENSP00000507786.1:p.His587Asp | |
| ENST00000683039.1:c.1759C>G | ENSP00000508303.1:p.His587Asp | |
| ENST00000683235.1:c.1759C>G | ENSP00000507646.1:p.His587Asp | |
| ENST00000683381.1:c.1759C>G | ENSP00000508184.1:p.His587Asp | |
| ENST00000684584.1:c.1252C>G | ENSP00000508044.1:p.His418Asp | |
| ENST00000259008.7:c.1759C>G MANE Select | ENSP00000259008.2:p.His587Asp | |
| ENST00000259008.6:c.1759C>G | ENSP00000259008.2:p.His587Asp | |
| ENST00000577598.5:c.1759C>G | ENSP00000464654.1:p.His587Asp | |
| ENST00000579028.1:c.452C>G | ||
| NM_032043.2:c.1759C>G , LRG_300t1:c.1759C>G | NP_114432.2:p.His587Asp | |
| XM_011525332.1:c.1759C>G | XP_011523634.1:p.His587Asp | |
| XM_011525333.1:c.1759C>G | XP_011523635.1:p.His587Asp | |
| XM_011525334.1:c.1759C>G | XP_011523636.1:p.His587Asp | |
| XM_011525335.1:c.1759C>G | XP_011523637.1:p.His587Asp | |
| XM_011525336.1:c.1759C>G | XP_011523638.1:p.His587Asp | |
| XM_011525337.1:c.1759C>G | XP_011523639.1:p.His587Asp | |
| XM_011525338.1:c.1276C>G | XP_011523640.1:p.His426Asp | |
| XM_011525339.1:c.1759C>G | XP_011523641.1:p.His587Asp | |
| XM_011525340.1:c.1759C>G | XP_011523642.1:p.His587Asp | |
| XM_011525341.1:c.1759C>G | XP_011523643.1:p.His587Asp | |
| XM_011525332.3:c.1759C>G | XP_011523634.1:p.His587Asp | |
| XM_011525333.3:c.1759C>G | XP_011523635.1:p.His587Asp | |
| XM_011525334.2:c.1759C>G | XP_011523636.1:p.His587Asp | |
| XM_011525335.3:c.1759C>G | XP_011523637.1:p.His587Asp | |
| XM_011525336.2:c.1759C>G | XP_011523638.1:p.His587Asp | |
| XM_011525337.2:c.1759C>G | XP_011523639.1:p.His587Asp | |
| XM_011525338.2:c.1276C>G | XP_011523640.1:p.His426Asp | |
| XM_011525339.3:c.1759C>G | XP_011523641.1:p.His587Asp | |
| XM_011525340.3:c.1759C>G | XP_011523642.1:p.His587Asp | |
| XM_011525341.3:c.1759C>G | XP_011523643.1:p.His587Asp | |
| XM_017025200.1:c.1276C>G | XP_016880689.1:p.His426Asp | |
| XM_017025201.1:c.1216C>G | XP_016880690.1:p.His406Asp | |
| NM_032043.3:c.1759C>G MANE Select | NP_114432.2:p.His587Asp |