Linked Data
ClinVar Variation Id:
471652
dbSNP Id:
rs534269714
ExAC:
8:144996303 G / A
gnomAD v2:
8-144996303-G-A
gnomAD v3:
8-143922135-G-A
gnomAD v4:
8-143922135-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143922135G>A , CM000670.2:g.143922135G>A | GRCh38 |
| NC_000008.10:g.144996303G>A , CM000670.1:g.144996303G>A | GRCh37 |
| NC_000008.9:g.145068291G>A | NCBI36 |
| NG_012492.1:g.59611C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.7818C>T | ENSP00000437303.2:p.Ala2606= | |
| ENST00000685198.1:c.7737C>T | ENSP00000510528.1:p.Ala2579= | |
| ENST00000687971.1:c.7404C>T | ENSP00000510788.1:p.Ala2468= | |
| ENST00000693060.1:c.7617C>T | ENSP00000510329.1:p.Ala2539= | |
| ENST00000345136.8:c.7686C>T MANE Select | ENSP00000344848.3:p.Ala2562= | |
| ENST00000527303.2:c.4386C>T | ENSP00000433982.2:p.Ala1462= | |
| ENST00000322810.8:c.8097C>T | ENSP00000323856.4:p.Ala2699= | |
| ENST00000345136.7:c.7686C>T | ENSP00000344848.3:p.Ala2562= | |
| ENST00000354589.7:c.7686C>T | ENSP00000346602.3:p.Ala2562= | |
| ENST00000354958.6:c.7620C>T | ENSP00000347044.2:p.Ala2540= | |
| ENST00000356346.7:c.7644C>T MANE Plus Clinical | ENSP00000348702.3:p.Ala2548= | |
| ENST00000357649.6:c.7698C>T | ENSP00000350277.2:p.Ala2566= | |
| ENST00000398774.6:c.7590C>T | ENSP00000381756.2:p.Ala2530= | |
| ENST00000436759.6:c.7767C>T | ENSP00000388180.2:p.Ala2589= | |
| ENST00000527096.5:c.7755C>T | ENSP00000434583.1:p.Ala2585= | |
| ENST00000527303.1:c.395C>T | ||
| NM_000445.4:c.7767C>T | NP_000436.2:p.Ala2589= | |
| NM_201378.3:c.7644C>T | NP_958780.1:p.Ala2548= | |
| NM_201379.2:c.7620C>T | NP_958781.1:p.Ala2540= | |
| NM_201380.3:c.8097C>T | NP_958782.1:p.Ala2699= | |
| NM_201381.2:c.7590C>T | NP_958783.1:p.Ala2530= | |
| NM_201382.3:c.7686C>T | NP_958784.1:p.Ala2562= | |
| NM_201383.2:c.7698C>T | NP_958785.1:p.Ala2566= | |
| NM_201384.2:c.7686C>T | NP_958786.1:p.Ala2562= | |
| XM_005250976.2:c.8112C>T | XP_005251033.1:p.Ala2704= | |
| XM_005250978.2:c.7713C>T | XP_005251035.1:p.Ala2571= | |
| XM_005250979.3:c.7701C>T | XP_005251036.1:p.Ala2567= | |
| XM_005250980.3:c.7701C>T | XP_005251037.1:p.Ala2567= | |
| XM_005250981.2:c.7659C>T | XP_005251038.1:p.Ala2553= | |
| XM_005250982.2:c.7635C>T | XP_005251039.1:p.Ala2545= | |
| XM_005250983.2:c.7617C>T | XP_005251040.1:p.Ala2539= | |
| XM_005250984.3:c.7605C>T | XP_005251041.1:p.Ala2535= | |
| XM_006716588.2:c.7782C>T | XP_006716651.1:p.Ala2594= | |
| XM_006716589.2:c.7632C>T | XP_006716652.1:p.Ala2544= | |
| XM_006716590.2:c.7632C>T | XP_006716653.1:p.Ala2544= | |
| XM_011517130.1:c.7701C>T | XP_011515432.1:p.Ala2567= | |
| XM_011517131.1:c.7617C>T | XP_011515433.1:p.Ala2539= | |
| XM_011517132.1:c.4332C>T | XP_011515434.1:p.Ala1444= | |
| XM_005250976.4:c.8112C>T | XP_005251033.1:p.Ala2704= | |
| XM_005250978.3:c.7713C>T | XP_005251035.1:p.Ala2571= | |
| XM_005250979.4:c.7701C>T | XP_005251036.1:p.Ala2567= | |
| XM_005250980.4:c.7701C>T | XP_005251037.1:p.Ala2567= | |
| XM_005250981.3:c.7659C>T | XP_005251038.1:p.Ala2553= | |
| XM_005250982.4:c.7635C>T | XP_005251039.1:p.Ala2545= | |
| XM_005250984.5:c.7605C>T | XP_005251041.1:p.Ala2535= | |
| XM_006716588.3:c.7782C>T | XP_006716651.1:p.Ala2594= | |
| XM_006716590.3:c.7632C>T | XP_006716653.1:p.Ala2544= | |
| XM_011517130.2:c.7701C>T | XP_011515432.1:p.Ala2567= | |
| XM_011517131.2:c.7617C>T | XP_011515433.1:p.Ala2539= | |
| XM_011517132.2:c.4332C>T | XP_011515434.1:p.Ala1444= | |
| NM_000445.5:c.7767C>T | NP_000436.2:p.Ala2589= | |
| NM_201378.4:c.7644C>T MANE Plus Clinical | NP_958780.1:p.Ala2548= | |
| NM_201379.3:c.7620C>T | NP_958781.1:p.Ala2540= | |
| NM_201380.4:c.8097C>T | NP_958782.1:p.Ala2699= | |
| NM_201381.3:c.7590C>T | NP_958783.1:p.Ala2530= | |
| NM_201382.4:c.7686C>T | NP_958784.1:p.Ala2562= | |
| NM_201383.3:c.7698C>T | NP_958785.1:p.Ala2566= | |
| NM_201384.3:c.7686C>T MANE Select | NP_958786.1:p.Ala2562= |