Linked Data
ClinVar Variation Id:
502659
dbSNP Id:
rs782527767
ExAC:
8:144990681 G / A
gnomAD v2:
8-144990681-G-A
gnomAD v3:
8-143916513-G-A
gnomAD v4:
8-143916513-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143916513G>A , CM000670.2:g.143916513G>A | GRCh38 |
| NC_000008.10:g.144990681G>A , CM000670.1:g.144990681G>A | GRCh37 |
| NC_000008.9:g.145062669G>A | NCBI36 |
| NG_012492.1:g.65233C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.13440C>T | ENSP00000437303.2:p.Thr4480= | |
| ENST00000685198.1:c.13359C>T | ENSP00000510528.1:p.Thr4453= | |
| ENST00000687971.1:c.13026C>T | ENSP00000510788.1:p.Thr4342= | |
| ENST00000693060.1:c.13239C>T | ENSP00000510329.1:p.Thr4413= | |
| ENST00000345136.8:c.13308C>T MANE Select | ENSP00000344848.3:p.Thr4436= | |
| ENST00000527303.2:c.10008C>T | ENSP00000433982.2:p.Thr3336= | |
| ENST00000322810.8:c.13719C>T | ENSP00000323856.4:p.Thr4573= | |
| ENST00000345136.7:c.13308C>T | ENSP00000344848.3:p.Thr4436= | |
| ENST00000354589.7:c.13308C>T | ENSP00000346602.3:p.Thr4436= | |
| ENST00000354958.6:c.13242C>T | ENSP00000347044.2:p.Thr4414= | |
| ENST00000356346.7:c.13266C>T MANE Plus Clinical | ENSP00000348702.3:p.Thr4422= | |
| ENST00000357649.6:c.13320C>T | ENSP00000350277.2:p.Thr4440= | |
| ENST00000398774.6:c.13212C>T | ENSP00000381756.2:p.Thr4404= | |
| ENST00000436759.6:c.13389C>T | ENSP00000388180.2:p.Thr4463= | |
| ENST00000527096.5:c.13377C>T | ENSP00000434583.1:p.Thr4459= | |
| NM_000445.4:c.13389C>T | NP_000436.2:p.Thr4463= | |
| NM_201378.3:c.13266C>T | NP_958780.1:p.Thr4422= | |
| NM_201379.2:c.13242C>T | NP_958781.1:p.Thr4414= | |
| NM_201380.3:c.13719C>T | NP_958782.1:p.Thr4573= | |
| NM_201381.2:c.13212C>T | NP_958783.1:p.Thr4404= | |
| NM_201382.3:c.13308C>T | NP_958784.1:p.Thr4436= | |
| NM_201383.2:c.13320C>T | NP_958785.1:p.Thr4440= | |
| NM_201384.2:c.13308C>T | NP_958786.1:p.Thr4436= | |
| XM_005250976.2:c.13734C>T | XP_005251033.1:p.Thr4578= | |
| XM_005250978.2:c.13335C>T | XP_005251035.1:p.Thr4445= | |
| XM_005250979.3:c.13323C>T | XP_005251036.1:p.Thr4441= | |
| XM_005250980.3:c.13323C>T | XP_005251037.1:p.Thr4441= | |
| XM_005250981.2:c.13281C>T | XP_005251038.1:p.Thr4427= | |
| XM_005250982.2:c.13257C>T | XP_005251039.1:p.Thr4419= | |
| XM_005250983.2:c.13239C>T | XP_005251040.1:p.Thr4413= | |
| XM_005250984.3:c.13227C>T | XP_005251041.1:p.Thr4409= | |
| XM_006716588.2:c.13404C>T | XP_006716651.1:p.Thr4468= | |
| XM_006716589.2:c.13254C>T | XP_006716652.1:p.Thr4418= | |
| XM_006716590.2:c.13254C>T | XP_006716653.1:p.Thr4418= | |
| XM_011517130.1:c.13323C>T | XP_011515432.1:p.Thr4441= | |
| XM_011517131.1:c.13239C>T | XP_011515433.1:p.Thr4413= | |
| XM_011517132.1:c.9954C>T | XP_011515434.1:p.Thr3318= | |
| XM_005250976.4:c.13734C>T | XP_005251033.1:p.Thr4578= | |
| XM_005250978.3:c.13335C>T | XP_005251035.1:p.Thr4445= | |
| XM_005250979.4:c.13323C>T | XP_005251036.1:p.Thr4441= | |
| XM_005250980.4:c.13323C>T | XP_005251037.1:p.Thr4441= | |
| XM_005250981.3:c.13281C>T | XP_005251038.1:p.Thr4427= | |
| XM_005250982.4:c.13257C>T | XP_005251039.1:p.Thr4419= | |
| XM_005250984.5:c.13227C>T | XP_005251041.1:p.Thr4409= | |
| XM_006716588.3:c.13404C>T | XP_006716651.1:p.Thr4468= | |
| XM_006716590.3:c.13254C>T | XP_006716653.1:p.Thr4418= | |
| XM_011517130.2:c.13323C>T | XP_011515432.1:p.Thr4441= | |
| XM_011517131.2:c.13239C>T | XP_011515433.1:p.Thr4413= | |
| XM_011517132.2:c.9954C>T | XP_011515434.1:p.Thr3318= | |
| NM_000445.5:c.13389C>T | NP_000436.2:p.Thr4463= | |
| NM_201378.4:c.13266C>T MANE Plus Clinical | NP_958780.1:p.Thr4422= | |
| NM_201379.3:c.13242C>T | NP_958781.1:p.Thr4414= | |
| NM_201380.4:c.13719C>T | NP_958782.1:p.Thr4573= | |
| NM_201381.3:c.13212C>T | NP_958783.1:p.Thr4404= | |
| NM_201382.4:c.13308C>T | NP_958784.1:p.Thr4436= | |
| NM_201383.3:c.13320C>T | NP_958785.1:p.Thr4440= | |
| NM_201384.3:c.13308C>T MANE Select | NP_958786.1:p.Thr4436= |