Linked Data
ClinVar Variation Id:
487434
dbSNP Id:
rs761639530
ExAC:
17:59763235 G / C
gnomAD v2:
17-59763235-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61685874G>C , CM000679.2:g.61685874G>C | GRCh38 |
| NC_000017.10:g.59763235G>C , CM000679.1:g.59763235G>C | GRCh37 |
| NC_000017.9:g.57118017G>C | NCBI36 |
| NG_007409.2:g.182686C>G , LRG_300:g.182686C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682066.1:c.2997C>G | ENSP00000507191.1:n.2997C>G | |
| ENST00000682073.1:n.1607C>G | ||
| ENST00000682433.1:n.1946C>G | ||
| ENST00000682453.1:c.2867C>G | ENSP00000506943.1:p.Ser956Ter | |
| ENST00000682477.1:c.*2293C>G | ENSP00000507075.1:n.*2293C>G | |
| ENST00000682589.1:n.8744C>G | ||
| ENST00000682755.1:c.2645C>G | ENSP00000507660.1:p.Ser882Ter | |
| ENST00000682989.1:c.2610-1734C>G | ENSP00000507786.1:n.2610-1734C>G | |
| ENST00000683039.1:c.2867C>G | ENSP00000508303.1:p.Ser956Ter | |
| ENST00000683235.1:c.*282C>G | ENSP00000507646.1:n.*282C>G | |
| ENST00000683535.1:n.997C>G | ||
| ENST00000684471.1:n.1280C>G | ||
| ENST00000684584.1:c.2069-1734C>G | ENSP00000508044.1:n.2069-1734C>G | |
| ENST00000684626.1:n.1113C>G | ||
| ENST00000684769.1:c.1057C>G | ENSP00000507691.1:n.1057C>G | |
| ENST00000259008.7:c.2867C>G MANE Select | ENSP00000259008.2:p.Ser956Ter | |
| ENST00000259008.6:c.2867C>G | ENSP00000259008.2:p.Ser956Ter | |
| ENST00000577598.5:c.2867C>G | ENSP00000464654.1:p.Ser956Ter | |
| NM_032043.2:c.2867C>G , LRG_300t1:c.2867C>G | NP_114432.2:p.Ser956Ter | |
| XM_011525332.1:c.2927C>G | XP_011523634.1:p.Ser976Ter | |
| XM_011525333.1:c.2927C>G | XP_011523635.1:p.Ser976Ter | |
| XM_011525334.1:c.2927C>G | XP_011523636.1:p.Ser976Ter | |
| XM_011525335.1:c.2867C>G | XP_011523637.1:p.Ser956Ter | |
| XM_011525336.1:c.2807C>G | XP_011523638.1:p.Ser936Ter | |
| XM_011525337.1:c.2726C>G | XP_011523639.1:p.Ser909Ter | |
| XM_011525338.1:c.2444C>G | XP_011523640.1:p.Ser815Ter | |
| XM_011525332.3:c.2927C>G | XP_011523634.1:p.Ser976Ter | |
| XM_011525333.3:c.2927C>G | XP_011523635.1:p.Ser976Ter | |
| XM_011525334.2:c.2927C>G | XP_011523636.1:p.Ser976Ter | |
| XM_011525335.3:c.2867C>G | XP_011523637.1:p.Ser956Ter | |
| XM_011525336.2:c.2807C>G | XP_011523638.1:p.Ser936Ter | |
| XM_011525337.2:c.2726C>G | XP_011523639.1:p.Ser909Ter | |
| XM_011525338.2:c.2444C>G | XP_011523640.1:p.Ser815Ter | |
| XM_017025200.1:c.2384C>G | XP_016880689.1:p.Ser795Ter | |
| XM_017025201.1:c.2384C>G | XP_016880690.1:p.Ser795Ter | |
| XM_017025202.1:c.1013C>G | XP_016880691.1:p.Ser338Ter | |
| XM_017025203.1:c.1013C>G | XP_016880692.1:p.Ser338Ter | |
| NM_032043.3:c.2867C>G MANE Select | NP_114432.2:p.Ser956Ter |